Product NDC: | 16590-186 |
Proprietary Name: | Phentermine Hydrochloride |
Non Proprietary Name: | Phentermine Hydrochloride |
Active Ingredient(s): | 37.5 mg/1 & nbsp; Phentermine Hydrochloride |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 16590-186 |
Labeler Name: | STAT Rx USA LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA040526 |
Marketing Category: | ANDA |
Start Marketing Date: | 20031023 |
Package NDC: | 16590-186-15 |
Package Description: | 15 TABLET in 1 BOTTLE, PLASTIC (16590-186-15) |
NDC Code | 16590-186-15 |
Proprietary Name | Phentermine Hydrochloride |
Package Description | 15 TABLET in 1 BOTTLE, PLASTIC (16590-186-15) |
Product NDC | 16590-186 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Phentermine Hydrochloride |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20031023 |
Marketing Category Name | ANDA |
Labeler Name | STAT Rx USA LLC |
Substance Name | PHENTERMINE HYDROCHLORIDE |
Strength Number | 37.5 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Appetite Suppression [PE],Increased Sympathetic Activity [PE],Sympathomimetic Amine Anorectic [EPC] |