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01 3Actavis Inc

02 1BUNDY

03 3HALSEY

04 2Hikma Pharmaceuticals

05 2IVAX Pharmaceuticals Inc

06 4Lannett Company, Inc.

07 2MARSHALL PHARMA

08 1Meda Pharmaceuticals Inc.

09 4NORVIUM BIOSCIENCE

10 4Sandoz B2B

11 4Solvay Chemicals International S.A

12 2Teva Pharmaceutical Industries

13 4Viatris

14 2WHITEWORTH TOWN PLSN

15 1Wockhardt

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PharmaCompass

01

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

BUTABARBITAL SODIUM

Brand Name : BUTABARBITAL SODIUM

Dosage Form : TABLET;ORAL

Dosage Strength : 15MG

Packaging :

Approval Date : 1982-01-01

Application Number : 85764

Regulatory Info : DISCN

Registration Country : USA

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02

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

BUTABARBITAL SODIUM

Brand Name : BUTABARBITAL SODIUM

Dosage Form : TABLET;ORAL

Dosage Strength : 30MG

Packaging :

Approval Date : 1982-01-01

Application Number : 85772

Regulatory Info : DISCN

Registration Country : USA

blank

03

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

BUTABARBITAL SODIUM

Brand Name : SODIUM BUTABARBITAL

Dosage Form : TABLET;ORAL

Dosage Strength : 15MG

Packaging :

Approval Date : 1982-01-01

Application Number : 85418

Regulatory Info : DISCN

Registration Country : USA

blank

04

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

BUTABARBITAL SODIUM

Brand Name : SODIUM BUTABARBITAL

Dosage Form : TABLET;ORAL

Dosage Strength : 30MG

Packaging :

Approval Date : 1982-01-01

Application Number : 85432

Regulatory Info : DISCN

Registration Country : USA

blank

05

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

BUTABARBITAL SODIUM

Brand Name : SODIUM BUTABARBITAL

Dosage Form : TABLET;ORAL

Dosage Strength : 15MG

Packaging :

Approval Date : 1982-01-01

Application Number : 83484

Regulatory Info : DISCN

Registration Country : USA

blank

06

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

BUTABARBITAL SODIUM

Brand Name : SODIUM BUTABARBITAL

Dosage Form : TABLET;ORAL

Dosage Strength : 30MG

Packaging :

Approval Date : 1982-01-01

Application Number : 84040

Regulatory Info : DISCN

Registration Country : USA

blank

07

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

BUTABARBITAL SODIUM

Brand Name : BUTISOL SODIUM

Dosage Form : ELIXIR;ORAL

Dosage Strength : 30MG/5ML

Packaging :

Approval Date : 1982-01-01

Application Number : 85380

Regulatory Info : DISCN

Registration Country : USA

blank

08

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

BUTABARBITAL SODIUM

Brand Name : BUTABARBITAL SODIUM

Dosage Form : TABLET;ORAL

Dosage Strength : 30MG

Packaging :

Approval Date : 1982-01-01

Application Number : 84272

Regulatory Info : DISCN

Registration Country : USA

blank

09

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

BUTABARBITAL SODIUM

Brand Name : BUTABARBITAL SODIUM

Dosage Form : TABLET;ORAL

Dosage Strength : 15MG

Packaging :

Approval Date : 1982-02-09

Application Number : 84292

Regulatory Info : DISCN

Registration Country : USA

blank

10

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

BUTABARBITAL SODIUM

Brand Name : BUTABARBITAL SODIUM

Dosage Form : TABLET;ORAL

Dosage Strength : 16.2MG

Packaging :

Approval Date : 1982-01-01

Application Number : 83606

Regulatory Info : DISCN

Registration Country : USA

blank

11

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

BUTABARBITAL SODIUM

Brand Name : BUTABARBITAL SODIUM

Dosage Form : TABLET;ORAL

Dosage Strength : 97.2MG

Packaging :

Approval Date : 1982-01-01

Application Number : 83896

Regulatory Info : DISCN

Registration Country : USA

blank

12

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

BUTABARBITAL SODIUM

Brand Name : BUTABARBITAL SODIUM

Dosage Form : TABLET;ORAL

Dosage Strength : 48.6MG

Packaging :

Approval Date : 1982-01-01

Application Number : 83897

Regulatory Info : DISCN

Registration Country : USA

blank

13

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

BUTABARBITAL SODIUM

Brand Name : BUTABARBITAL SODIUM

Dosage Form : TABLET;ORAL

Dosage Strength : 32.4MG

Packaging :

Approval Date : 1982-01-01

Application Number : 83898

Regulatory Info : DISCN

Registration Country : USA

blank

14

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

BUTABARBITAL SODIUM

Brand Name : BUTICAPS

Dosage Form : CAPSULE;ORAL

Dosage Strength : 15MG

Packaging :

Approval Date : 1982-01-01

Application Number : 85381

Regulatory Info : DISCN

Registration Country : USA

blank

15

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

BUTABARBITAL SODIUM

Brand Name : BUTICAPS

Dosage Form : CAPSULE;ORAL

Dosage Strength : 30MG

Packaging :

Approval Date : 1982-01-01

Application Number : 85381

Regulatory Info : DISCN

Registration Country : USA

blank

16

Pharmtech & Ingredients
Not Confirmed
arrow
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Pharmtech & Ingredients
Not Confirmed

BUTABARBITAL SODIUM

Brand Name : BUTICAPS

Dosage Form : CAPSULE;ORAL

Dosage Strength : 50MG

Packaging :

Approval Date : 1982-01-01

Application Number : 85381

Regulatory Info : DISCN

Registration Country : USA

blank

17

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

BUTABARBITAL SODIUM

Brand Name : BUTICAPS

Dosage Form : CAPSULE;ORAL

Dosage Strength : 100MG

Packaging :

Approval Date : 1982-01-01

Application Number : 85381

Regulatory Info : DISCN

Registration Country : USA

blank

18

Pharmtech & Ingredients
Not Confirmed
arrow
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Pharmtech & Ingredients
Not Confirmed

BUTABARBITAL SODIUM

Brand Name : BUTABARBITAL SODIUM

Dosage Form : ELIXIR;ORAL

Dosage Strength : 30MG/5ML

Packaging :

Approval Date : 1982-01-01

Application Number : 85383

Regulatory Info : DISCN

Registration Country : USA

blank

19

NORVIUM BIOSCIENCE

Country
Pharmtech & Ingredients
Not Confirmed
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NORVIUM BIOSCIENCE

Country
arrow
Pharmtech & Ingredients
Not Confirmed

BUTABARBITAL SODIUM

Brand Name : BUTISOL SODIUM

Dosage Form : TABLET;ORAL

Dosage Strength : 15MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 1982-01-01

Application Number : 793

Regulatory Info : DISCN

Registration Country : USA

blank

20

NORVIUM BIOSCIENCE

Country
Pharmtech & Ingredients
Not Confirmed
arrow

NORVIUM BIOSCIENCE

Country
arrow
Pharmtech & Ingredients
Not Confirmed

BUTABARBITAL SODIUM

Brand Name : BUTISOL SODIUM

Dosage Form : TABLET;ORAL

Dosage Strength : 50MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 1982-01-01

Application Number : 793

Regulatory Info : DISCN

Registration Country : USA

blank

21

NORVIUM BIOSCIENCE

Country
Pharmtech & Ingredients
Not Confirmed
arrow

NORVIUM BIOSCIENCE

Country
arrow
Pharmtech & Ingredients
Not Confirmed

BUTABARBITAL SODIUM

Brand Name : BUTISOL SODIUM

Dosage Form : TABLET;ORAL

Dosage Strength : 30MG

Packaging :

Approval Date : 1982-01-01

Application Number : 793

Regulatory Info : DISCN

Registration Country : USA

blank

22

NORVIUM BIOSCIENCE

Country
Pharmtech & Ingredients
Not Confirmed
arrow

NORVIUM BIOSCIENCE

Country
arrow
Pharmtech & Ingredients
Not Confirmed

BUTABARBITAL SODIUM

Brand Name : BUTISOL SODIUM

Dosage Form : TABLET;ORAL

Dosage Strength : 100MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 1982-01-01

Application Number : 793

Regulatory Info : DISCN

Registration Country : USA

blank

23

WHITEWORTH TOWN PLSN

Country
Pharmtech & Ingredients
Not Confirmed
arrow

WHITEWORTH TOWN PLSN

Country
arrow
Pharmtech & Ingredients
Not Confirmed

BUTABARBITAL SODIUM

Brand Name : BUTABARBITAL SODIUM

Dosage Form : TABLET;ORAL

Dosage Strength : 15MG

Packaging :

Approval Date : 1982-01-01

Application Number : 83325

Regulatory Info : DISCN

Registration Country : USA

blank

24

WHITEWORTH TOWN PLSN

Country
Pharmtech & Ingredients
Not Confirmed
arrow

WHITEWORTH TOWN PLSN

Country
arrow
Pharmtech & Ingredients
Not Confirmed

BUTABARBITAL SODIUM

Brand Name : BUTABARBITAL SODIUM

Dosage Form : TABLET;ORAL

Dosage Strength : 30MG

Packaging :

Approval Date : 1982-01-01

Application Number : 83337

Regulatory Info : DISCN

Registration Country : USA

blank

25

MARSHALL PHARMA

Country
Pharmtech & Ingredients
Not Confirmed
arrow

MARSHALL PHARMA

Country
arrow
Pharmtech & Ingredients
Not Confirmed

BUTABARBITAL SODIUM

Brand Name : SODIUM BUTABARBITAL

Dosage Form : TABLET;ORAL

Dosage Strength : 16.2MG

Packaging :

Approval Date : 1982-01-01

Application Number : 83524

Regulatory Info : DISCN

Registration Country : USA

blank

26

MARSHALL PHARMA

Country
Pharmtech & Ingredients
Not Confirmed
arrow

MARSHALL PHARMA

Country
arrow
Pharmtech & Ingredients
Not Confirmed

BUTABARBITAL SODIUM

Brand Name : SODIUM BUTABARBITAL

Dosage Form : TABLET;ORAL

Dosage Strength : 32.4MG

Packaging :

Approval Date : 1982-01-01

Application Number : 83858

Regulatory Info : DISCN

Registration Country : USA

blank

27

HALSEY

Country
Pharmtech & Ingredients
Not Confirmed
arrow

HALSEY

Country
arrow
Pharmtech & Ingredients
Not Confirmed

BUTABARBITAL SODIUM

Brand Name : SARISOL NO. 1

Dosage Form : TABLET;ORAL

Dosage Strength : 15MG

Packaging :

Approval Date : 1982-01-01

Application Number : 84719

Regulatory Info : DISCN

Registration Country : USA

blank

28

HALSEY

Country
Pharmtech & Ingredients
Not Confirmed
arrow

HALSEY

Country
arrow
Pharmtech & Ingredients
Not Confirmed

BUTABARBITAL SODIUM

Brand Name : SARISOL NO. 2

Dosage Form : TABLET;ORAL

Dosage Strength : 30MG

Packaging :

Approval Date : 1982-01-01

Application Number : 84719

Regulatory Info : DISCN

Registration Country : USA

blank

29

HALSEY

Country
Pharmtech & Ingredients
Not Confirmed
arrow

HALSEY

Country
arrow
Pharmtech & Ingredients
Not Confirmed

BUTABARBITAL SODIUM

Brand Name : SARISOL

Dosage Form : ELIXIR;ORAL

Dosage Strength : 30MG/5ML

Packaging :

Approval Date : 1982-01-01

Application Number : 84723

Regulatory Info : DISCN

Registration Country : USA

blank

30

BUNDY

Country
Pharmtech & Ingredients
Not Confirmed
arrow

BUNDY

Country
arrow
Pharmtech & Ingredients
Not Confirmed

BUTABARBITAL SODIUM

Brand Name : BUTABARBITAL

Dosage Form : TABLET;ORAL

Dosage Strength : 30MG

Packaging :

Approval Date : 1982-01-01

Application Number : 85550

Regulatory Info : DISCN

Registration Country : USA

blank