Seconal Sodium (Valeant Pharmaceuticals North America LLC)
Welcome to the PulseAid listing for the Seconal Sodium drug offered from Valeant Pharmaceuticals North America LLC. This pharmaceutical is classified as a HUMAN PRESCRIPTION DRUG. Below, you can view details for this drug, such as its dosage form, route of delivery, start market/end market dates, and more. We have also randomly listed additional pharmaceuticals used in the same HUMAN PRESCRIPTION DRUG drug type category.
LABELER NAME / MANUFACTURER: | Valeant Pharmaceuticals North America LLC |
NON-PROPRIETARY NAME: | secobarbital sodium |
SUBSTANCE NAME: | SECOBARBITAL SODIUM |
TYPE: | HUMAN PRESCRIPTION DRUG |
PHARMA CLASS: | |
ROUTE: | ORAL |
DOSAGE FORM: | CAPSULE |
MARKETING CATEGORY NAME: | ANDA |
START MARKETING DATE: | 1983-10-03 |
END MARKETING DATE: | 0000-00-00 |
Seconal Sodium HUMAN PRESCRIPTION DRUG Details:
Item Description | Seconal Sodium from Valeant Pharmaceuticals North America LLC |
LABELER NAME: | Valeant Pharmaceuticals North America LLC |
DEA SCHEDULE: | CII
|
ACTIVE STRENGTH: | 100(mg/1) |
START MARKETING DATE: | 1983-10-03 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 0187-4220_d892a312-12ba-4d32-a840-2c0ff3dc1d58 |
PRODUCT NDC: | 0187-4220 |
APPLICATION NUMBER: | ANDA086101 |
Other SECOBARBITAL SODIUM Pharmaceutical Manufacturers / Labelers: