Benzphetamine Hydrochloride is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Aidarex Pharmaceuticals Llc. The primary component is Benzphetamine Hydrochloride.
| Product ID | 53217-175_3904530d-83e6-4359-b6a9-63f15b0366f1 |
| NDC | 53217-175 |
| Product Type | Human Prescription Drug |
| Proprietary Name | Benzphetamine Hydrochloride |
| Generic Name | Benzphetamine Hydrochloride |
| Dosage Form | Tablet |
| Route of Administration | ORAL |
| Marketing Start Date | 2010-09-07 |
| Marketing Category | ANDA / ANDA |
| Application Number | ANDA040747 |
| Labeler Name | Aidarex Pharmaceuticals LLC |
| Substance Name | BENZPHETAMINE HYDROCHLORIDE |
| Active Ingredient Strength | 50 mg/1 |
| Pharm Classes | Appetite Suppression [PE],Increased Sympathetic Activity [PE],Sympathomimetic Amine Anorectic [EPC] |
| DEA Schedule | CIII |
| NDC Exclude Flag | N |
| Listing Certified Through | 2019-12-31 |
| Marketing Start Date | 2010-09-07 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | ANDA |
| Application Number | ANDA040747 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2010-09-07 |
| Inactivation Date | 2020-01-31 |
| Marketing Category | ANDA |
| Application Number | ANDA040747 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2010-09-07 |
| Inactivation Date | 2020-01-31 |
| Marketing Category | ANDA |
| Application Number | ANDA040747 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2010-09-07 |
| Inactivation Date | 2020-01-31 |
| Marketing Category | ANDA |
| Application Number | ANDA040747 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2010-09-07 |
| Inactivation Date | 2020-01-31 |
| Marketing Category | ANDA |
| Application Number | ANDA040747 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2010-09-07 |
| Inactivation Date | 2020-01-31 |
| Marketing Category | ANDA |
| Application Number | ANDA040747 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2010-09-07 |
| Inactivation Date | 2020-01-31 |
| Ingredient | Strength |
|---|---|
| BENZPHETAMINE HYDROCHLORIDE | 50 mg/1 |
| SPL SET ID: | 5ca0eee3-8f84-4ee2-b339-c9cdbf6ffd52 |
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI |