Active Ingredient: BUTABARBITAL SODIUM
Proprietary Name: BUTABARBITAL SODIUM
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 30MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A088631
Product Number: 001
Approval Date: May 1, 1985
Applicant Holder Full Name: TEVA PHARMACEUTICALS USA INC
Marketing Status:
Discontinued
Patent and Exclusivity Information