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01 3Dr. Reddy's Laboratories

02 2ADAPTIS

03 2American Regent

04 2Amneal Pharmaceuticals

05 2Amphastar Pharmaceuticals

06 2Amring Pharma

07 4Aurobindo Pharma Limited

08 2Avet Pharmaceuticals

09 4Biological E

10 2Caplin Point Laboratories Limited

11 2ENDO OPERATIONS

12 3Exela Pharma Sciences, LLC.

13 8Farbe Firma

14 3Fresenius Kabi USA

15 2Fresenius SE & Co. KGaA

16 2GLAND PHARMA LIMITED

17 1Grindeks AS

18 1Hanlim Pharmaceuticals Inc

19 3Hikma Pharmaceuticals

20 1JAMP PHARMA

21 1Labiana Life Sciences S.A

22 1Lifespan Biotech

23 2MARCAN PHARMACEUTICALS INC

24 2Meitheal Pharmaceuticals

25 3Omega Laboratories Limited

26 2Pharmascience Inc.

27 2Pluviaendo

28 1Polifarma

29 2Sagent Pharmaceuticals

30 2Umedica Laboratories

31 1Winston Medical Supply

32 1Zhejiang Xianju Pharmaceutical Co. Ltd

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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 : RX

Registration Country : USA

NEOSTIGMINE METHYLSULFATE

Brand Name : NEOSTIGMINE METHYLSULFATE

Dosage Form : SOLUTION;INTRAVENOUS

Dosage Strength : 5MG/10ML (0.5MG/ML)

Packaging :

Approval Date : 2018-07-10

Application Number : 209135

Regulatory Info : RX

Registration Country : USA

Dr Reddy Company Banner

02

  • fda
  • EDQM
  • WHO-GMP

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

Regulatory Info : RX

Registration Country : USA

NEOSTIGMINE METHYLSULFATE

Brand Name : NEOSTIGMINE METHYLSULFATE

Dosage Form : SOLUTION;INTRAVENOUS

Dosage Strength : 10MG/10ML (1MG/ML)

Packaging :

Approval Date : 2018-07-10

Application Number : 209135

Regulatory Info : RX

Registration Country : USA

Dr Reddy Company Banner

03

  • fda
  • EDQM
  • WHO-GMP

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

Regulatory Info : RX

Registration Country : USA

NEOSTIGMINE METHYLSULFATE

Brand Name : NEOSTIGMINE METHYLSULFATE

Dosage Form : SOLUTION;INTRAVENOUS

Dosage Strength : 3MG/3ML (1MG/ML)

Packaging :

Approval Date : 2022-07-06

Application Number : 216291

Regulatory Info : RX

Registration Country : USA

Dr Reddy Company Banner

04

2024 ACI Convention
Not Confirmed
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2024 ACI Convention
Not Confirmed

NEOSTIGMINE METHYLSULFATE

Brand Name : NEOSTIGMINE METHYLSULFATE

Dosage Form : SOLUTION;INTRAVENOUS

Dosage Strength : 5MG/10ML (0.5MG/ML)

Packaging :

Approval Date : 2018-05-04

Application Number : 209182

Regulatory Info : DISCN

Registration Country : USA

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05

2024 ACI Convention
Not Confirmed
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2024 ACI Convention
Not Confirmed

NEOSTIGMINE METHYLSULFATE

Brand Name : NEOSTIGMINE METHYLSULFATE

Dosage Form : SOLUTION;INTRAVENOUS

Dosage Strength : 10MG/10ML (1MG/ML)

Packaging :

Approval Date : 2018-05-04

Application Number : 209182

Regulatory Info : DISCN

Registration Country : USA

blank

06

2024 ACI Convention
Not Confirmed
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2024 ACI Convention
Not Confirmed

NEOSTIGMINE METHYLSULFATE

Brand Name : NEOSTIGMINE METHYLSULFATE

Dosage Form : SOLUTION;INTRAVENOUS

Dosage Strength : 5MG/10ML (0.5MG/ML)

Packaging :

Approval Date : 2018-06-15

Application Number : 210051

Regulatory Info : RX

Registration Country : USA

blank

07

2024 ACI Convention
Not Confirmed
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2024 ACI Convention
Not Confirmed

NEOSTIGMINE METHYLSULFATE

Brand Name : NEOSTIGMINE METHYLSULFATE

Dosage Form : SOLUTION;INTRAVENOUS

Dosage Strength : 5MG/10ML (0.5MG/ML)

Packaging :

Approval Date : 2017-09-25

Application Number : 209933

Regulatory Info : RX

Registration Country : USA

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08

2024 ACI Convention
Not Confirmed
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2024 ACI Convention
Not Confirmed

NEOSTIGMINE METHYLSULFATE

Brand Name : NEOSTIGMINE METHYLSULFATE

Dosage Form : SOLUTION;INTRAVENOUS

Dosage Strength : 10MG/10ML (1MG/ML)

Packaging :

Approval Date : 2017-09-25

Application Number : 209933

Regulatory Info : RX

Registration Country : USA

blank

09

2024 ACI Convention
Not Confirmed
arrow
arrow
2024 ACI Convention
Not Confirmed

NEOSTIGMINE METHYLSULFATE

Brand Name : NEOSTIGMINE METHYSULFATE

Dosage Form : SOLUTION;INTRAVENOUS

Dosage Strength : 5MG/10ML (0.5MG/ML)

Packaging :

Approval Date : 2022-11-25

Application Number : 208230

Regulatory Info : RX

Registration Country : USA

blank

10

2024 ACI Convention
Not Confirmed
arrow
arrow
2024 ACI Convention
Not Confirmed

NEOSTIGMINE METHYLSULFATE

Brand Name : NEOSTIGMINE METHYSULFATE

Dosage Form : SOLUTION;INTRAVENOUS

Dosage Strength : 10MG/10ML (1MG/ML)

Packaging :

Approval Date : 2022-11-25

Application Number : 208230

Regulatory Info : RX

Registration Country : USA

blank

11

2024 ACI Convention
Not Confirmed
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2024 ACI Convention
Not Confirmed

NEOSTIGMINE METHYLSULFATE

Brand Name : BLOXIVERZ

Dosage Form : SOLUTION;INTRAVENOUS

Dosage Strength : 5MG/10ML (0.5MG/ML)

Packaging :

Approval Date : 2013-05-31

Application Number : 204078

Regulatory Info : RX

Registration Country : USA

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12

2024 ACI Convention
Not Confirmed
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2024 ACI Convention
Not Confirmed

NEOSTIGMINE METHYLSULFATE

Brand Name : BLOXIVERZ

Dosage Form : SOLUTION;INTRAVENOUS

Dosage Strength : 10MG/10ML (1MG/ML)

Packaging :

Approval Date : 2013-05-31

Application Number : 204078

Regulatory Info : RX

Registration Country : USA

blank

13

2024 ACI Convention
Not Confirmed
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2024 ACI Convention
Not Confirmed

NEOSTIGMINE METHYLSULFATE

Brand Name : BLOXIVERZ

Dosage Form : SOLUTION;INTRAVENOUS

Dosage Strength : 5MG/5ML (1MG/ML)

Packaging :

Approval Date : 2023-10-27

Application Number : 204078

Regulatory Info : DISCN

Registration Country : USA

blank

14

2024 ACI Convention
Not Confirmed
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2024 ACI Convention
Not Confirmed

NEOSTIGMINE METHYLSULFATE

Brand Name : NEOSTIGMINE METHYLSULFATE

Dosage Form : SOLUTION;INTRAVENOUS

Dosage Strength : 5MG/10ML (0.5MG/ML)

Packaging :

Approval Date : 2015-01-08

Application Number : 203629

Regulatory Info : RX

Registration Country : USA

blank

15

2024 ACI Convention
Not Confirmed
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arrow
2024 ACI Convention
Not Confirmed

NEOSTIGMINE METHYLSULFATE

Brand Name : NEOSTIGMINE METHYLSULFATE

Dosage Form : SOLUTION;INTRAVENOUS

Dosage Strength : 10MG/10ML (1MG/ML)

Packaging :

Approval Date : 2015-01-08

Application Number : 203629

Regulatory Info : RX

Registration Country : USA

blank

16

2024 ACI Convention
Not Confirmed
arrow
arrow
2024 ACI Convention
Not Confirmed

NEOSTIGMINE METHYLSULFATE

Brand Name : NEOSTIGMINE METHYLSULFATE

Dosage Form : SOLUTION;INTRAVENOUS

Dosage Strength : 3MG/3ML (1MG/ML)

Packaging :

Approval Date : 2018-09-18

Application Number : 203629

Regulatory Info : RX

Registration Country : USA

blank

17

2024 ACI Convention
Not Confirmed
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2024 ACI Convention
Not Confirmed

NEOSTIGMINE METHYLSULFATE

Brand Name : NEOSTIGMINE METHYLSULFATE

Dosage Form : SOLUTION;INTRAVENOUS

Dosage Strength : 5MG/10ML (0.5MG/ML)

Packaging :

Approval Date : 2015-12-28

Application Number : 207042

Regulatory Info : RX

Registration Country : USA

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18

2024 ACI Convention
Not Confirmed
arrow
arrow
2024 ACI Convention
Not Confirmed

NEOSTIGMINE METHYLSULFATE

Brand Name : NEOSTIGMINE METHYLSULFATE

Dosage Form : SOLUTION;INTRAVENOUS

Dosage Strength : 10MG/10ML (1MG/ML)

Packaging :

Approval Date : 2015-12-28

Application Number : 207042

Regulatory Info : RX

Registration Country : USA

blank

19

ENDO OPERATIONS

Country
2024 ACI Convention
Not Confirmed
arrow

ENDO OPERATIONS

Country
arrow
2024 ACI Convention
Not Confirmed

NEOSTIGMINE METHYLSULFATE

Brand Name : NEOSTIGMINE METHYLSULFATE

Dosage Form : SOLUTION;INTRAVENOUS

Dosage Strength : 5MG/10ML (0.5MG/ML)

Packaging :

Approval Date : 2017-04-26

Application Number : 208405

Regulatory Info : RX

Registration Country : USA

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20

ENDO OPERATIONS

Country
2024 ACI Convention
Not Confirmed
arrow

ENDO OPERATIONS

Country
arrow
2024 ACI Convention
Not Confirmed

NEOSTIGMINE METHYLSULFATE

Brand Name : NEOSTIGMINE METHYLSULFATE

Dosage Form : SOLUTION;INTRAVENOUS

Dosage Strength : 10MG/10ML (1MG/ML)

Packaging :

Approval Date : 2017-04-26

Application Number : 208405

Regulatory Info : RX

Registration Country : USA

blank