Product NDC: | 0115-1205 |
Proprietary Name: | Benzphetamine Hydrochloride |
Non Proprietary Name: | Benzphetamine Hydrochloride |
Active Ingredient(s): | 50 mg/1 & nbsp; Benzphetamine Hydrochloride |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0115-1205 |
Labeler Name: | Global Pharmaceuticals, Division of Impax Laboratories Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA040845 |
Marketing Category: | ANDA |
Start Marketing Date: | 20081201 |
Package NDC: | 0115-1205-13 |
Package Description: | 90 TABLET in 1 BOTTLE (0115-1205-13) |
NDC Code | 0115-1205-13 |
Proprietary Name | Benzphetamine Hydrochloride |
Package Description | 90 TABLET in 1 BOTTLE (0115-1205-13) |
Product NDC | 0115-1205 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Benzphetamine Hydrochloride |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20081201 |
Marketing Category Name | ANDA |
Labeler Name | Global Pharmaceuticals, Division of Impax Laboratories Inc. |
Substance Name | BENZPHETAMINE HYDROCHLORIDE |
Strength Number | 50 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Appetite Suppression [PE],Increased Sympathetic Activity [PE],Sympathomimetic Amine Anorectic [EPC] |