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 |