Product NDC: | 63629-2949 |
Proprietary Name: | Phentermine Hydrochloride |
Non Proprietary Name: | Phentermine Hydrochloride |
Active Ingredient(s): | 30 mg/1 & nbsp; Phentermine Hydrochloride |
Administration Route(s): | ORAL |
Dosage Form(s): | CAPSULE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 63629-2949 |
Labeler Name: | Bryant Ranch Prepack |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA087022 |
Marketing Category: | ANDA |
Start Marketing Date: | 20071201 |
Package NDC: | 63629-2949-1 |
Package Description: | 30 CAPSULE in 1 BOTTLE (63629-2949-1) |
NDC Code | 63629-2949-1 |
Proprietary Name | Phentermine Hydrochloride |
Package Description | 30 CAPSULE in 1 BOTTLE (63629-2949-1) |
Product NDC | 63629-2949 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Phentermine Hydrochloride |
Dosage Form Name | CAPSULE |
Route Name | ORAL |
Start Marketing Date | 20071201 |
Marketing Category Name | ANDA |
Labeler Name | Bryant Ranch Prepack |
Substance Name | PHENTERMINE HYDROCHLORIDE |
Strength Number | 30 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Appetite Suppression [PE],Increased Sympathetic Activity [PE],Sympathomimetic Amine Anorectic [EPC] |