FDA
Sodium Butabarbital
The FDA lists this product in 9 strengths and forms.
Composition
- Active ingredients
- BUTABARBITAL SODIUM 30MG
Strengths and forms
The FDA lists each strength of a product separately; these pages share one label.
- BUTABARBITAL SODIUM 15MG · TabletANDA085849-001 · Discontinued
- BUTABARBITAL SODIUM 15MG · TabletANDA085418-001 · Discontinued
- BUTABARBITAL SODIUM 30MG · TabletANDA084040-001 · Discontinued
- BUTABARBITAL SODIUM 30MG · TabletANDA085866-001 · Discontinued
- BUTABARBITAL SODIUM 15MG · TabletANDA083484-001 · Discontinued
- BUTABARBITAL SODIUM 100MG · TabletANDA085881-001 · Discontinued
- BUTABARBITAL SODIUM 32.4MG · TabletANDA083858-001 · Discontinued
- BUTABARBITAL SODIUM 16.2MG · TabletANDA083524-001 · Discontinued
- BUTABARBITAL SODIUM 30MG · TabletThis page
Official product information
Drugs@FDA lists the approved labels, letters and reviews for application ANDA085432.
At a glance
- Brand name
- Sodium Butabarbital
- Active substance
- butabarbital sodium
- Route
- Oral
- Dosage form
- Tablet
- Applicant
- Hikma
- Status
- Discontinued
- FDA approval
- 20 Dec 1977
- Application
- ANDA085432-001