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01 1Actavis Inc

02 1Anabolic Laboratories

03 2BIMEDA-MTC ANIMAL HEALTH INC

04 1BPI Labs

05 1Bausch Health

06 2ELKINS SINN

07 3Epic Pharma. LLC.

08 1HALSEY

09 1Hanlim Pharmaceuticals Inc

10 1Hikma Pharmaceuticals

11 2IVAX Pharmaceuticals Inc

12 2Lannett Company, Inc.

13 1Nexgen Pharma, Inc.

14 1PUREPAC PHARM

15 1Perrigo Company plc

16 1Pfizer Inc

17 1RAFTER 8 PRODUCTS INC

18 1Rising Pharmaceuticals Inc

19 1Sagent Pharmaceuticals

20 5ScieGen Pharmaceuticals

21 2VITARINE

22 1WHITEWORTH TOWN PLSN

23 2Wyeth Pharmaceuticals Inc

24 1everyLIFE Technologies

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PharmaCompass

01

Fi Europe 2024
Not Confirmed
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Fi Europe 2024
Not Confirmed

PENTOBARBITAL SODIUM

Brand Name : SODIUM PENTOBARBITAL

Dosage Form : CAPSULE;ORAL

Dosage Strength : 100MG

Packaging :

Approval Date : 1982-01-01

Application Number : 85791

Regulatory Info : DISCN

Registration Country : USA

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02

Fi Europe 2024
Not Confirmed
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Fi Europe 2024
Not Confirmed

PENTOBARBITAL SODIUM

Brand Name : SODIUM PENTOBARBITAL

Dosage Form : CAPSULE;ORAL

Dosage Strength : 100MG

Packaging :

Approval Date : 1982-01-01

Application Number : 84590

Regulatory Info : DISCN

Registration Country : USA

blank

03

Fi Europe 2024
Not Confirmed
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Fi Europe 2024
Not Confirmed

PENTOBARBITAL SODIUM

Brand Name : SODIUM PENTOBARBITAL

Dosage Form : CAPSULE;ORAL

Dosage Strength : 100MG

Packaging :

Approval Date : 1982-01-01

Application Number : 83264

Regulatory Info : DISCN

Registration Country : USA

blank

04

Fi Europe 2024
Not Confirmed
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Fi Europe 2024
Not Confirmed

PENTOBARBITAL SODIUM

Brand Name : NEMBUTAL SODIUM

Dosage Form : CAPSULE;ORAL

Dosage Strength : 100MG

Packaging :

Approval Date : 1982-01-01

Application Number : 83245

Regulatory Info : DISCN

Registration Country : USA

blank

05

Fi Europe 2024
Not Confirmed
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Fi Europe 2024
Not Confirmed

PENTOBARBITAL SODIUM

Brand Name : NEMBUTAL SODIUM

Dosage Form : CAPSULE;ORAL

Dosage Strength : 50MG

Packaging :

Approval Date : 1982-01-01

Application Number : 84093

Regulatory Info : DISCN

Registration Country : USA

blank

06

Fi Europe 2024
Not Confirmed
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Fi Europe 2024
Not Confirmed

PENTOBARBITAL SODIUM

Brand Name : NEMBUTAL SODIUM

Dosage Form : CAPSULE;ORAL

Dosage Strength : 30MG

Packaging :

Approval Date : 1982-01-01

Application Number : 84095

Regulatory Info : DISCN

Registration Country : USA

blank

07

Fi Europe 2024
Not Confirmed
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Fi Europe 2024
Not Confirmed

PENTOBARBITAL SODIUM

Brand Name : SODIUM PENTOBARBITAL

Dosage Form : CAPSULE;ORAL

Dosage Strength : 100MG

Packaging :

Approval Date : 1982-01-01

Application Number : 83259

Regulatory Info : DISCN

Registration Country : USA

blank

08

Fi Europe 2024
Not Confirmed
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Fi Europe 2024
Not Confirmed

PENTOBARBITAL SODIUM

Brand Name : PENTOBARBITAL SODIUM

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 50MG/ML

Packaging :

Approval Date : 2017-11-13

Application Number : 203619

Regulatory Info : RX

Registration Country : USA

blank

09

Fi Europe 2024
Not Confirmed
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Fi Europe 2024
Not Confirmed

PENTOBARBITAL SODIUM

Brand Name : SODIUM PENTOBARBITAL

Dosage Form : CAPSULE;ORAL

Dosage Strength : 50MG

Packaging :

Approval Date : 1982-01-01

Application Number : 83461

Regulatory Info : DISCN

Registration Country : USA

blank

10

Fi Europe 2024
Not Confirmed
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Fi Europe 2024
Not Confirmed

PENTOBARBITAL SODIUM

Brand Name : SODIUM PENTOBARBITAL

Dosage Form : CAPSULE;ORAL

Dosage Strength : 100MG

Packaging :

Approval Date : 1982-01-01

Application Number : 83461

Regulatory Info : DISCN

Registration Country : USA

blank

11

Fi Europe 2024
Not Confirmed
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Fi Europe 2024
Not Confirmed

PENTOBARBITAL SODIUM

Brand Name : PENTOBARBITAL SODIUM

Dosage Form : CAPSULE;ORAL

Dosage Strength : 100MG

Packaging :

Approval Date : 1982-01-01

Application Number : 85915

Regulatory Info : DISCN

Registration Country : USA

blank

12

Fi Europe 2024
Not Confirmed
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Fi Europe 2024
Not Confirmed

PENTOBARBITAL SODIUM

Brand Name : PENTOBARBITAL SODIUM

Dosage Form : CAPSULE;ORAL

Dosage Strength : 50MG

Packaging :

Approval Date : 1982-01-01

Application Number : 85937

Regulatory Info : DISCN

Registration Country : USA

blank

13

Fi Europe 2024
Not Confirmed
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Fi Europe 2024
Not Confirmed

PENTOBARBITAL SODIUM

Brand Name : SODIUM PENTOBARBITAL

Dosage Form : TABLET;ORAL

Dosage Strength : 100MG

Packaging :

Approval Date : 1982-01-01

Application Number : 84238

Regulatory Info : DISCN

Registration Country : USA

blank

14

Fi Europe 2024
Not Confirmed
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Fi Europe 2024
Not Confirmed

PENTOBARBITAL SODIUM

Brand Name : SODIUM PENTOBARBITAL

Dosage Form : CAPSULE;ORAL

Dosage Strength : 100MG

Packaging :

Approval Date : 1982-01-01

Application Number : 84560

Regulatory Info : DISCN

Registration Country : USA

blank

15

Fi Europe 2024
Not Confirmed
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Fi Europe 2024
Not Confirmed

PENTOBARBITAL SODIUM

Brand Name : SODIUM PENTOBARBITAL

Dosage Form : CAPSULE;ORAL

Dosage Strength : 100MG

Packaging :

Approval Date : 1982-01-01

Application Number : 84156

Regulatory Info : DISCN

Registration Country : USA

blank

16

Fi Europe 2024
Not Confirmed
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Fi Europe 2024
Not Confirmed

PENTOBARBITAL SODIUM

Brand Name : SODIUM PENTOBARBITAL

Dosage Form : CAPSULE;ORAL

Dosage Strength : 100MG

Packaging :

Approval Date : 1982-01-01

Application Number : 83301

Regulatory Info : DISCN

Registration Country : USA

blank

17

Fi Europe 2024
Not Confirmed
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Fi Europe 2024
Not Confirmed

PENTOBARBITAL SODIUM

Brand Name : NEMBUTAL SODIUM

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 50MG/ML

Packaging :

Approval Date : 1982-01-01

Application Number : 83246

Regulatory Info : RX

Registration Country : USA

blank

18

Fi Europe 2024
Not Confirmed
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Fi Europe 2024
Not Confirmed

PENTOBARBITAL

Brand Name : NEMBUTAL

Dosage Form : ELIXIR;ORAL

Dosage Strength : 18.2MG/5ML

Packaging :

Approval Date : 1982-01-01

Application Number : 83244

Regulatory Info : DISCN

Registration Country : USA

blank

19

Fi Europe 2024
Not Confirmed
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Fi Europe 2024
Not Confirmed

PENTOBARBITAL SODIUM

Brand Name : NEMBUTAL

Dosage Form : SUPPOSITORY;RECTAL

Dosage Strength : 30MG

Packaging :

Approval Date : 1982-01-25

Application Number : 83247

Regulatory Info : DISCN

Registration Country : USA

blank

20

Fi Europe 2024
Not Confirmed
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Fi Europe 2024
Not Confirmed

PENTOBARBITAL SODIUM

Brand Name : NEMBUTAL

Dosage Form : SUPPOSITORY;RECTAL

Dosage Strength : 60MG

Packaging :

Approval Date : 1982-01-25

Application Number : 83247

Regulatory Info : DISCN

Registration Country : USA

blank

21

Fi Europe 2024
Not Confirmed
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Fi Europe 2024
Not Confirmed

PENTOBARBITAL SODIUM

Brand Name : NEMBUTAL

Dosage Form : SUPPOSITORY;RECTAL

Dosage Strength : 120MG

Packaging :

Approval Date : 1982-01-25

Application Number : 83247

Regulatory Info : DISCN

Registration Country : USA

blank

22

Fi Europe 2024
Not Confirmed
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Fi Europe 2024
Not Confirmed

PENTOBARBITAL SODIUM

Brand Name : NEMBUTAL

Dosage Form : SUPPOSITORY;RECTAL

Dosage Strength : 200MG

Packaging :

Approval Date : 1982-01-25

Application Number : 83247

Regulatory Info : DISCN

Registration Country : USA

blank

23

Fi Europe 2024
Not Confirmed
arrow
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Fi Europe 2024
Not Confirmed

PENTOBARBITAL SODIUM

Brand Name : SODIUM PENTOBARBITAL

Dosage Form : CAPSULE;ORAL

Dosage Strength : 100MG

Packaging :

Approval Date : 1982-01-01

Application Number : 83239

Regulatory Info : DISCN

Registration Country : USA

blank

24

Fi Europe 2024
Not Confirmed
arrow
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Fi Europe 2024
Not Confirmed

PENTOBARBITAL SODIUM

Brand Name : SODIUM PENTOBARBITAL

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 50MG/ML

Packaging :

Approval Date : 1982-01-01

Application Number : 83261

Regulatory Info : DISCN

Registration Country : USA

blank

25

ELKINS SINN

Country
Fi Europe 2024
Not Confirmed
arrow

ELKINS SINN

Country
arrow
Fi Europe 2024
Not Confirmed

PENTOBARBITAL SODIUM

Brand Name : PENTOBARBITAL SODIUM

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 50MG/ML

Packaging :

Approval Date : 1982-01-01

Application Number : 83270

Regulatory Info : DISCN

Registration Country : USA

blank

26

VITARINE

Country
Fi Europe 2024
Not Confirmed
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VITARINE

Country
arrow
Fi Europe 2024
Not Confirmed

PENTOBARBITAL SODIUM

Brand Name : PENTOBARBITAL SODIUM

Dosage Form : CAPSULE;ORAL

Dosage Strength : 100MG

Packaging :

Approval Date : 1982-01-01

Application Number : 83284

Regulatory Info : DISCN

Registration Country : USA

blank

27

VITARINE

Country
Fi Europe 2024
Not Confirmed
arrow

VITARINE

Country
arrow
Fi Europe 2024
Not Confirmed

PENTOBARBITAL SODIUM

Brand Name : PENTOBARBITAL SODIUM

Dosage Form : TABLET;ORAL

Dosage Strength : 100MG

Packaging :

Approval Date : 1982-01-01

Application Number : 83285

Regulatory Info : DISCN

Registration Country : USA

blank

28

WHITEWORTH TOWN PLSN

Country
Fi Europe 2024
Not Confirmed
arrow

WHITEWORTH TOWN PLSN

Country
arrow
Fi Europe 2024
Not Confirmed

PENTOBARBITAL SODIUM

Brand Name : PENTOBARBITAL SODIUM

Dosage Form : CAPSULE;ORAL

Dosage Strength : 100MG

Packaging :

Approval Date : 1982-01-01

Application Number : 83338

Regulatory Info : DISCN

Registration Country : USA

blank

29

ELKINS SINN

Country
Fi Europe 2024
Not Confirmed
arrow

ELKINS SINN

Country
arrow
Fi Europe 2024
Not Confirmed

PENTOBARBITAL SODIUM

Brand Name : SODIUM PENTOBARBITAL

Dosage Form : CAPSULE;ORAL

Dosage Strength : 100MG

Packaging :

Approval Date : 1982-01-01

Application Number : 83368

Regulatory Info : DISCN

Registration Country : USA

blank

30

HALSEY

Country
Fi Europe 2024
Not Confirmed
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HALSEY

Country
arrow
Fi Europe 2024
Not Confirmed

PENTOBARBITAL SODIUM

Brand Name : SODIUM PENTOBARBITAL

Dosage Form : CAPSULE;ORAL

Dosage Strength : 100MG

Packaging :

Approval Date : 1982-01-01

Application Number : 84677

Regulatory Info : DISCN

Registration Country : USA

blank