Product NDC: | 63629-3051 |
Proprietary Name: | Phendimetrazine Tartrate |
Non Proprietary Name: | Phendimetrazine Tartrate |
Active Ingredient(s): | 105 mg/1 & nbsp; Phendimetrazine Tartrate |
Administration Route(s): | ORAL |
Dosage Form(s): | CAPSULE, EXTENDED RELEASE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 63629-3051 |
Labeler Name: | Bryant Ranch Prepack |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA018074 |
Marketing Category: | NDA |
Start Marketing Date: | 19770906 |
Package NDC: | 63629-3051-5 |
Package Description: | 2 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (63629-3051-5) |
NDC Code | 63629-3051-5 |
Proprietary Name | Phendimetrazine Tartrate |
Package Description | 2 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (63629-3051-5) |
Product NDC | 63629-3051 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Phendimetrazine Tartrate |
Dosage Form Name | CAPSULE, EXTENDED RELEASE |
Route Name | ORAL |
Start Marketing Date | 19770906 |
Marketing Category Name | NDA |
Labeler Name | Bryant Ranch Prepack |
Substance Name | PHENDIMETRAZINE TARTRATE |
Strength Number | 105 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Appetite Suppression [PE],Increased Sympathetic Activity [PE],Sympathomimetic Amine Anorectic [EPC] |