Composition
- Active ingredients
- BUTABARBITAL SODIUM 50MG
Strengths and forms
The FDA lists each strength of a product separately; these pages share one label.
Official product information
Drugs@FDA lists the approved labels, letters and reviews for application ANDA085381.
Prognia shows this product information for reference and learning. It is not treatment advice and can lag behind the official text. Always check the current product information and local protocols before prescribing.
At a glance
- Brand name
- Buticaps
- Active substance
- butabarbital sodium
- Route
- Oral
- Dosage form
- Capsule
- Applicant
- Medpointe Pharm HLC
- Status
- Discontinued
- FDA approval
- 11 Apr 1978
- Application
- ANDA085381-003