NDC Code | 68071-2171-9 |
Package Description | 90 TABLET in 1 BOTTLE (68071-2171-9) |
Product NDC | 68071-2171 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Diethylpropion Hydrochloride |
Non-Proprietary Name | Diethylpropion Hydrochloride |
Dosage Form | TABLET |
Usage | ORAL |
Start Marketing Date | 20110718 |
Marketing Category Name | ANDA |
Application Number | ANDA200177 |
Manufacturer | NuCare Pharmaceuticals, Inc. |
Substance Name | DIETHYLPROPION HYDROCHLORIDE |
Strength | 25 |
Strength Unit | mg/1 |
Pharmacy Classes | Appetite Suppression [PE],Increased Sympathetic Activity [PE],Sympathomimetic Amine Anorectic [EPC] |
DEA Schedule | CIV |