Product NDC: | 54868-0283 |
Proprietary Name: | PHENTERMINE HYDROCHLORIDE |
Non Proprietary Name: | phentermine hydrochloride |
Active Ingredient(s): | 15 mg/1 & nbsp; phentermine hydrochloride |
Administration Route(s): | ORAL |
Dosage Form(s): | CAPSULE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 54868-0283 |
Labeler Name: | Physicians Total Care, inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA040886 |
Marketing Category: | ANDA |
Start Marketing Date: | 19970428 |
Package NDC: | 54868-0283-0 |
Package Description: | 30 CAPSULE in 1 BOTTLE (54868-0283-0) |
NDC Code | 54868-0283-0 |
Proprietary Name | PHENTERMINE HYDROCHLORIDE |
Package Description | 30 CAPSULE in 1 BOTTLE (54868-0283-0) |
Product NDC | 54868-0283 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | phentermine hydrochloride |
Dosage Form Name | CAPSULE |
Route Name | ORAL |
Start Marketing Date | 19970428 |
Marketing Category Name | ANDA |
Labeler Name | Physicians Total Care, inc. |
Substance Name | PHENTERMINE HYDROCHLORIDE |
Strength Number | 15 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Appetite Suppression [PE],Increased Sympathetic Activity [PE],Sympathomimetic Amine Anorectic [EPC] |