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01 1Dr. Reddy's Laboratories

02 3Strides Pharma Science

03 1ANI Pharmaceuticals Inc

04 2Actavis Inc

05 1Ascot Pharma

06 1Bausch Health

07 1Chartwell Pharmaceuticals llc

08 1Forest Laboratories

09 2Fosun Pharmaceutical

10 1GD Searle LLC

11 1HALSEY

12 1HEATHER

13 2Hikma Pharmaceuticals

14 2Johnson & Johnson

15 1KV Pharmaceutical

16 1Lannett Company, Inc.

17 2Leading Pharma, LLC

18 1MD Pharmaceutical

19 1Mallinckrodt Pharmaceuticals

20 1NORVIUM BIOSCIENCE

21 1PVT FORM

22 3Pfizer Inc

23 1ROXANE

24 1RP SCHERER GMBH & CO. KG

25 1SUPERPHARM

26 2Sun Pharmaceutical Industries Limited

27 1USL PHARMA

28 1Unichem Pharmaceuticals USA, Inc

29 1Upsher-Smith Laboratories

30 1VANGARD

31 2Viatris

32 1Winder Lab

33 1XYZ Pharma

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PharmaCompass

01

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothDRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.

Regulatory Info : DISCN

Registration Country : USA

ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE

Brand Name : DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE

Dosage Form : TABLET;ORAL

Dosage Strength : 0.025MG;2.5MG

Packaging :

Approval Date : 2020-06-03

Application Number : 210789

Regulatory Info : DISCN

Registration Country : USA

Dr Reddy Company Banner

02

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothStrides Pharma Science: Pioneering IP-driven formulations for niche finished dosage forms.

Regulatory Info : DISCN

Registration Country : USA

ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE

Brand Name : DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE

Dosage Form : TABLET;ORAL

Dosage Strength : 0.025MG;2.5MG

Packaging :

Approval Date : 2000-05-02

Application Number : 40357

Regulatory Info : DISCN

Registration Country : USA

Strides Pharma Science

03

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothStrides Pharma Science: Pioneering IP-driven formulations for niche finished dosage forms.

Regulatory Info :

Registration Country : India

Atropine Sulfate; Diphenoxylate Hydrochloride

Brand Name :

Dosage Form : Tablet

Dosage Strength : 2.5MG; 0.025MG

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : India

Strides Pharma Science

04

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothStrides Pharma Science: Pioneering IP-driven formulations for niche finished dosage forms.

Regulatory Info :

Registration Country : India

Diphenoxylate Hydrochloride; Atropine Sulfate

Brand Name :

Dosage Form : Tablet

Dosage Strength : 2.5MG; 0.025MG

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : India

Strides Pharma Science

05

AACR Annual meeting
Not Confirmed
arrow
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AACR Annual meeting
Not Confirmed

ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE

Brand Name : LOMANATE

Dosage Form : SOLUTION;ORAL

Dosage Strength : 0.025MG/5ML;2.5MG/5ML

Packaging :

Approval Date : 1982-01-01

Application Number : 85746

Regulatory Info : DISCN

Registration Country : USA

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06

AACR Annual meeting
Not Confirmed
arrow
arrow
AACR Annual meeting
Not Confirmed

ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE

Brand Name : DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE

Dosage Form : TABLET;ORAL

Dosage Strength : 0.025MG;2.5MG

Packaging :

Approval Date : 1982-01-01

Application Number : 85876

Regulatory Info : DISCN

Registration Country : USA

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07

AACR Annual meeting
Not Confirmed
arrow
arrow
AACR Annual meeting
Not Confirmed

ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE

Brand Name : DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE

Dosage Form : TABLET;ORAL

Dosage Strength : 0.025MG;2.5MG

Packaging :

Approval Date : 1982-01-01

Application Number : 86727

Regulatory Info : DISCN

Registration Country : USA

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08

AACR Annual meeting
Not Confirmed
arrow
arrow
AACR Annual meeting
Not Confirmed

ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE

Brand Name : DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE

Dosage Form : TABLET;ORAL

Dosage Strength : 0.025MG;2.5MG

Packaging :

Approval Date : 1982-02-16

Application Number : 87195

Regulatory Info : DISCN

Registration Country : USA

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09

AACR Annual meeting
Not Confirmed
arrow
arrow
AACR Annual meeting
Not Confirmed

ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE

Brand Name : DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE

Dosage Form : TABLET;ORAL

Dosage Strength : 0.025MG;2.5MG

Packaging :

Approval Date : 1982-01-01

Application Number : 85509

Regulatory Info : DISCN

Registration Country : USA

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10

AACR Annual meeting
Not Confirmed
arrow
arrow
AACR Annual meeting
Not Confirmed

ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE

Brand Name : LONOX

Dosage Form : TABLET;ORAL

Dosage Strength : 0.025MG;2.5MG

Packaging :

Approval Date : 1982-01-01

Application Number : 85311

Regulatory Info : DISCN

Registration Country : USA

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11

AACR Annual meeting
Not Confirmed
arrow
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AACR Annual meeting
Not Confirmed

ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE

Brand Name : DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE

Dosage Form : TABLET;ORAL

Dosage Strength : 0.025MG;2.5MG

Packaging :

Approval Date : 1982-01-01

Application Number : 86173

Regulatory Info : DISCN

Registration Country : USA

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12

AACR Annual meeting
Not Confirmed
arrow
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AACR Annual meeting
Not Confirmed

ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE

Brand Name : LOMOTIL

Dosage Form : SOLUTION;ORAL

Dosage Strength : 0.025MG/5ML;2.5MG/5ML

Packaging :

Approval Date : 1982-01-01

Application Number : 12699

Regulatory Info : DISCN

Registration Country : USA

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13

AACR Annual meeting
Not Confirmed
arrow
arrow
AACR Annual meeting
Not Confirmed

ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE

Brand Name : DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE

Dosage Form : SOLUTION;ORAL

Dosage Strength : 0.025MG/5ML;2.5MG/5ML

Packaging :

Approval Date : 1982-05-03

Application Number : 87708

Regulatory Info : RX

Registration Country : USA

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14

AACR Annual meeting
Not Confirmed
arrow
arrow
AACR Annual meeting
Not Confirmed

ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE

Brand Name : DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE

Dosage Form : TABLET;ORAL

Dosage Strength : 0.025MG;2.5MG

Packaging :

Approval Date : 1982-01-01

Application Number : 85659

Regulatory Info : DISCN

Registration Country : USA

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15

AACR Annual meeting
Not Confirmed
arrow
arrow
AACR Annual meeting
Not Confirmed

ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE

Brand Name : DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE

Dosage Form : TABLET;ORAL

Dosage Strength : 0.025MG;2.5MG

Packaging :

Approval Date : 1982-01-01

Application Number : 85372

Regulatory Info : RX

Registration Country : USA

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16

AACR Annual meeting
Not Confirmed
arrow
arrow
AACR Annual meeting
Not Confirmed

ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE

Brand Name : DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE

Dosage Form : TABLET;ORAL

Dosage Strength : 0.025MG;2.5MG

Packaging :

Approval Date : 1982-01-01

Application Number : 86950

Regulatory Info : DISCN

Registration Country : USA

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17

AACR Annual meeting
Not Confirmed
arrow
arrow
AACR Annual meeting
Not Confirmed

ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE

Brand Name : DI-ATRO

Dosage Form : TABLET;ORAL

Dosage Strength : 0.025MG;2.5MG

Packaging :

Approval Date : 1982-01-01

Application Number : 85266

Regulatory Info : DISCN

Registration Country : USA

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18

AACR Annual meeting
Not Confirmed
arrow
arrow
AACR Annual meeting
Not Confirmed

ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE

Brand Name : LOMOTIL

Dosage Form : TABLET;ORAL

Dosage Strength : 0.025MG;2.5MG

Packaging :

Approval Date : 1982-01-01

Application Number : 12462

Regulatory Info : RX

Registration Country : USA

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19

AACR Annual meeting
Not Confirmed
arrow
arrow
AACR Annual meeting
Not Confirmed

ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE

Brand Name : DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE

Dosage Form : TABLET;ORAL

Dosage Strength : 0.025MG;2.5MG

Packaging :

Approval Date : 1982-01-01

Application Number : 87131

Regulatory Info : DISCN

Registration Country : USA

blank

20

PVT FORM

Country
AACR Annual meeting
Not Confirmed
arrow

PVT FORM

Country
arrow
AACR Annual meeting
Not Confirmed

ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE

Brand Name : DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE

Dosage Form : TABLET;ORAL

Dosage Strength : 0.025MG;2.5MG

Packaging :

Approval Date : 1982-01-01

Application Number : 85766

Regulatory Info : DISCN

Registration Country : USA

blank

21

AACR Annual meeting
Not Confirmed
arrow
arrow
AACR Annual meeting
Not Confirmed

ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE

Brand Name : DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE

Dosage Form : TABLET;ORAL

Dosage Strength : 0.025MG;2.5MG

Packaging :

Approval Date : 1982-01-01

Application Number : 86057

Regulatory Info : DISCN

Registration Country : USA

blank

22

AACR Annual meeting
Not Confirmed
arrow
arrow
AACR Annual meeting
Not Confirmed

ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE

Brand Name : DIPHENOXYLATE HYDROCHLORIDE W/ ATROPINE SULFATE

Dosage Form : CAPSULE;ORAL

Dosage Strength : 0.025MG;2.5MG

Packaging :

Approval Date : 1982-01-01

Application Number : 86440

Regulatory Info : DISCN

Registration Country : USA

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23

AACR Annual meeting
Not Confirmed
arrow
arrow
AACR Annual meeting
Not Confirmed

ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE

Brand Name : DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE

Dosage Form : TABLET;ORAL

Dosage Strength : 0.025MG;2.5MG

Packaging :

Approval Date : 2000-11-27

Application Number : 40395

Regulatory Info : DISCN

Registration Country : USA

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24

AACR Annual meeting
Not Confirmed
arrow
arrow
AACR Annual meeting
Not Confirmed

ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE

Brand Name : DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE

Dosage Form : TABLET;ORAL

Dosage Strength : 0.025MG;2.5MG

Packaging :

Approval Date : 1982-01-01

Application Number : 85506

Regulatory Info : DISCN

Registration Country : USA

blank

25

AACR Annual meeting
Not Confirmed
arrow
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AACR Annual meeting
Not Confirmed

ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE

Brand Name : COLONAID

Dosage Form : SOLUTION;ORAL

Dosage Strength : 0.025MG/5ML;2.5MG/5ML

Packaging :

Approval Date : 1982-01-01

Application Number : 85735

Regulatory Info : DISCN

Registration Country : USA

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26

AACR Annual meeting
Not Confirmed
arrow
arrow
AACR Annual meeting
Not Confirmed

ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE

Brand Name : COLONAID

Dosage Form : TABLET;ORAL

Dosage Strength : 0.025MG;2.5MG

Packaging :

Approval Date : 1982-01-01

Application Number : 85737

Regulatory Info : DISCN

Registration Country : USA

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27

XYZ Pharma

AACR Annual meeting
Not Confirmed
arrow

XYZ Pharma

arrow
AACR Annual meeting
Not Confirmed

ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE

Brand Name : DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE

Dosage Form : TABLET;ORAL

Dosage Strength : 0.025MG;2.5MG

Packaging :

Approval Date : 1982-01-01

Application Number : 85035

Regulatory Info : DISCN

Registration Country : USA

blank

28

HALSEY

Country
AACR Annual meeting
Not Confirmed
arrow

HALSEY

Country
arrow
AACR Annual meeting
Not Confirmed

ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE

Brand Name : LOW-QUEL

Dosage Form : TABLET;ORAL

Dosage Strength : 0.025MG;2.5MG

Packaging :

Approval Date : 1982-01-01

Application Number : 85211

Regulatory Info : DISCN

Registration Country : USA

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29

NORVIUM BIOSCIENCE

Country
AACR Annual meeting
Not Confirmed
arrow

NORVIUM BIOSCIENCE

Country
arrow
AACR Annual meeting
Not Confirmed

ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE

Brand Name : DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE

Dosage Form : TABLET;ORAL

Dosage Strength : 0.025MG;2.5MG

Packaging :

Approval Date : 1982-01-01

Application Number : 85762

Regulatory Info : DISCN

Registration Country : USA

blank

30

HEATHER

Country
AACR Annual meeting
Not Confirmed
arrow

HEATHER

Country
arrow
AACR Annual meeting
Not Confirmed

ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE

Brand Name : DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE

Dosage Form : TABLET;ORAL

Dosage Strength : 0.025MG;2.5MG

Packaging :

Approval Date : 1982-01-01

Application Number : 86798

Regulatory Info : DISCN

Registration Country : USA

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