01 1ALPHARMA US PHARMS
02 1BUNDY
03 3HALSEY
04 2HIKMA
05 2IVAX SUB TEVA PHARMS
06 4LANNETT
07 2MARSHALL PHARMA
08 1MEDA PHARMS
09 4MEDPOINTE PHARM HLC
10 4NORVIUM BIOSCIENCE
11 4SANDOZ
12 4SOLVAY
13 2TEVA
14 2WATSON LABS
15 2WHITEWORTH TOWN PLSN
16 1WOCKHARDT
01 4CAPSULE;ORAL
02 5ELIXIR;ORAL
03 30TABLET;ORAL
01 39DISCN
01 1BUTABARB
02 1BUTABARBITAL
03 15BUTABARBITAL SODIUM
04 1BUTALAN
05 4BUTICAPS
06 5BUTISOL SODIUM
07 1SARISOL
08 1SARISOL NO. 1
09 1SARISOL NO. 2
10 9SODIUM BUTABARBITAL
01 37No
02 2Yes
RLD : No
TE Code :
Brand Name : SODIUM BUTABARBITAL
Dosage Form : TABLET;ORAL
Dosage Strength : 15MG
Approval Date : 1982-01-01
Application Number : 83484
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Brand Name : BUTABARBITAL SODIUM
Dosage Form : TABLET;ORAL
Dosage Strength : 16.2MG
Approval Date : 1982-01-01
Application Number : 83606
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
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Dosage Strength : 15MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1982-01-01
Application Number : 793
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
RLD : No
TE Code :
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Dosage Strength : 50MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1982-01-01
Application Number : 793
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
RLD : Yes
TE Code :
Brand Name : BUTISOL SODIUM
Dosage Form : TABLET;ORAL
Dosage Strength : 30MG
Approval Date : 1982-01-01
Application Number : 793
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
RLD : No
TE Code :
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Dosage Strength : 100MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1982-01-01
Application Number : 793
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
RLD : No
TE Code :
Brand Name : BUTABARBITAL SODIUM
Dosage Form : TABLET;ORAL
Dosage Strength : 15MG
Approval Date : 1982-01-01
Application Number : 83325
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
RLD : No
TE Code :
Brand Name : BUTABARBITAL SODIUM
Dosage Form : TABLET;ORAL
Dosage Strength : 30MG
Approval Date : 1982-01-01
Application Number : 83337
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
RLD : No
TE Code :
Brand Name : SODIUM BUTABARBITAL
Dosage Form : TABLET;ORAL
Dosage Strength : 16.2MG
Approval Date : 1982-01-01
Application Number : 83524
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
RLD : No
TE Code :
Brand Name : SODIUM BUTABARBITAL
Dosage Form : TABLET;ORAL
Dosage Strength : 32.4MG
Approval Date : 1982-01-01
Application Number : 83858
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
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