Product NDC: | 16590-642 |
Proprietary Name: | PHENDIMETRAZINE TARTRATE |
Non Proprietary Name: | PHENDIMETRAZINE TARTRATE |
Active Ingredient(s): | 35 mg/1 & nbsp; PHENDIMETRAZINE TARTRATE |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 16590-642 |
Labeler Name: | STAT RX USA LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA085588 |
Marketing Category: | ANDA |
Start Marketing Date: | 19770819 |
Package NDC: | 16590-642-60 |
Package Description: | 60 TABLET in 1 BOTTLE (16590-642-60) |
NDC Code | 16590-642-60 |
Proprietary Name | PHENDIMETRAZINE TARTRATE |
Package Description | 60 TABLET in 1 BOTTLE (16590-642-60) |
Product NDC | 16590-642 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | PHENDIMETRAZINE TARTRATE |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 19770819 |
Marketing Category Name | ANDA |
Labeler Name | STAT RX USA LLC |
Substance Name | PHENDIMETRAZINE TARTRATE |
Strength Number | 35 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Appetite Suppression [PE],Increased Sympathetic Activity [PE],Sympathomimetic Amine Anorectic [EPC] |