Please Wait
Applying Filters...
Menu
$ API Ref.Price (USD/KG) : 548Xls
Filters Filter
Cross PopUp
FILTER :

filter clear-filterReset all filters

01 1Dr. Reddy's Laboratories

02 3Strides Pharma Science

03 1ANI Pharmaceuticals Inc

04 2Actavis Inc

05 1Ascot Pharma

06 1Bausch Health

07 1Bayshore Pharmaceuticals

08 1Chartwell Pharmaceuticals llc

09 1DMFs Not Supported

10 1Forest Laboratories

11 2Fosun Pharmaceutical

12 1GD Searle LLC

13 1HALSEY

14 1HEATHER

15 2Hikma Pharmaceuticals

16 2Johnson & Johnson

17 1KV Pharmaceutical

18 1Lannett Company, Inc.

19 2Leading Pharma, LLC

20 1MD Pharmaceutical

21 1Mallinckrodt Pharmaceuticals

22 1PVT FORM

23 3Pfizer Inc

24 1ROXANE

25 1RP SCHERER GMBH & CO. KG

26 1SUPERPHARM

27 2Sun Pharmaceutical Industries Limited

28 1USL PHARMA

29 1Upsher-Smith Laboratories

30 3Viatris

31 1Winder Lab

32 1XYZ Pharma

filter clear-filterReset all filters

filter clear-filterReset all filters

filter clear-filterReset all filters

filter clear-filterReset all filters

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

Pharmtech & Ingredients
Not Confirmed
arrow
arrow
Pharmtech & Ingredients
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

blank

06

Pharmtech & Ingredients
Not Confirmed
arrow
arrow
Pharmtech & Ingredients
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

blank

07

Pharmtech & Ingredients
Not Confirmed
arrow
arrow
Pharmtech & Ingredients
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

blank

08

Pharmtech & Ingredients
Not Confirmed
arrow
arrow
Pharmtech & Ingredients
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

blank

09

Pharmtech & Ingredients
Not Confirmed
arrow
arrow
Pharmtech & Ingredients
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

blank

10

Pharmtech & Ingredients
Not Confirmed
arrow
arrow
Pharmtech & Ingredients
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

blank

11

Pharmtech & Ingredients
Not Confirmed
arrow
arrow
Pharmtech & Ingredients
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

blank

12

Pharmtech & Ingredients
Not Confirmed
arrow
arrow
Pharmtech & Ingredients
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

blank

13

Pharmtech & Ingredients
Not Confirmed
arrow
arrow
Pharmtech & Ingredients
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

blank

14

Pharmtech & Ingredients
Not Confirmed
arrow
arrow
Pharmtech & Ingredients
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

blank

15

Pharmtech & Ingredients
Not Confirmed
arrow
arrow
Pharmtech & Ingredients
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

blank

16

Pharmtech & Ingredients
Not Confirmed
arrow
arrow
Pharmtech & Ingredients
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

blank

17

Pharmtech & Ingredients
Not Confirmed
arrow
arrow
Pharmtech & Ingredients
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

blank

18

Pharmtech & Ingredients
Not Confirmed
arrow
arrow
Pharmtech & Ingredients
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

blank

19

Pharmtech & Ingredients
Not Confirmed
arrow
arrow
Pharmtech & Ingredients
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
Pharmtech & Ingredients
Not Confirmed
arrow

PVT FORM

Country
arrow
Pharmtech & Ingredients
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

Pharmtech & Ingredients
Not Confirmed
arrow
arrow
Pharmtech & Ingredients
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

Pharmtech & Ingredients
Not Confirmed
arrow
arrow
Pharmtech & Ingredients
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

blank

23

Pharmtech & Ingredients
Not Confirmed
arrow
arrow
Pharmtech & Ingredients
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

blank

24

Pharmtech & Ingredients
Not Confirmed
arrow
arrow
Pharmtech & Ingredients
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

Pharmtech & Ingredients
Not Confirmed
arrow
arrow
Pharmtech & Ingredients
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

blank

26

Pharmtech & Ingredients
Not Confirmed
arrow
arrow
Pharmtech & Ingredients
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

blank

27

Pharmtech & Ingredients
Not Confirmed
arrow
arrow
Pharmtech & Ingredients
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

28

XYZ Pharma

Pharmtech & Ingredients
Not Confirmed
arrow

XYZ Pharma

arrow
Pharmtech & Ingredients
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

29

HALSEY

Country
Pharmtech & Ingredients
Not Confirmed
arrow

HALSEY

Country
arrow
Pharmtech & Ingredients
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

blank

30

HEATHER

Country
Pharmtech & Ingredients
Not Confirmed
arrow

HEATHER

Country
arrow
Pharmtech & Ingredients
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

blank