Home
>
National Drug Code (NDC)
>
Benzphetamine Hydrochloride
Benzphetamine Hydrochloride - 23155-174-01 - (Benzphetamine Hydrochloride Tablets)
Drug Information of Benzphetamine Hydrochloride
| Product NDC: | 23155-174 |
| Proprietary Name: | Benzphetamine Hydrochloride |
| Non Proprietary Name: | Benzphetamine Hydrochloride Tablets |
| Active Ingredient(s): | 50 mg/1 & nbsp; Benzphetamine Hydrochloride Tablets |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Benzphetamine Hydrochloride
| Product NDC: | 23155-174 |
| Labeler Name: | Heritage Pharmaceuticals Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA202061 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20121019 |
Package Information of Benzphetamine Hydrochloride
| Package NDC: | 23155-174-01 |
| Package Description: | 100 TABLET, FILM COATED in 1 BOTTLE (23155-174-01) |
NDC Information of Benzphetamine Hydrochloride
| NDC Code | 23155-174-01 |
| Proprietary Name | Benzphetamine Hydrochloride |
| Package Description | 100 TABLET, FILM COATED in 1 BOTTLE (23155-174-01) |
| Product NDC | 23155-174 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Benzphetamine Hydrochloride Tablets |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20121019 |
| Marketing Category Name | ANDA |
| Labeler Name | Heritage Pharmaceuticals 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] |
