Amytal Sodium (Valeant Pharmaceuticals North America LLC)


Welcome to the PulseAid listing for the Amytal 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: amobarbital sodium
SUBSTANCE NAME: AMOBARBITAL SODIUM
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS:
ROUTE: INTRAMUSCULAR; INTRAVENOUS
DOSAGE FORM: INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
MARKETING CATEGORY NAME: UNAPPROVED DRUG OTHER
START MARKETING DATE: 2008-09-25
END MARKETING DATE: 0000-00-00


Amytal Sodium HUMAN PRESCRIPTION DRUG Details:

Item DescriptionAmytal Sodium from Valeant Pharmaceuticals North America LLC
LABELER NAME: Valeant Pharmaceuticals North America LLC
DEA SCHEDULE: CII
ACTIVE STRENGTH: 0.5(g/5mL)
START MARKETING DATE: 2008-09-25
END MARKETING DATE: 0000-00-00
PRODUCT ID: 0187-4303_94ba4d57-e4da-4080-9c8e-9e0065aef659
PRODUCT NDC: 0187-4303
APPLICATION NUMBER:

Other AMOBARBITAL SODIUM Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Valeant Pharmaceuticals North America LLCAmytal Sodium