Product NDC: | 12634-691 |
Proprietary Name: | DIETHYLPROPION HYDROCHLORIDE ER |
Non Proprietary Name: | DIETHYLPROPION HYDROCHLORIDE ER |
Active Ingredient(s): | 75 mg/1 & nbsp; DIETHYLPROPION HYDROCHLORIDE ER |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 12634-691 |
Labeler Name: | Apotheca Inc |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA011722 |
Marketing Category: | ANDA |
Start Marketing Date: | 20081023 |
Package NDC: | 12634-691-91 |
Package Description: | 1 TABLET in 1 BLISTER PACK (12634-691-91) |
NDC Code | 12634-691-91 |
Proprietary Name | DIETHYLPROPION HYDROCHLORIDE ER |
Package Description | 1 TABLET in 1 BLISTER PACK (12634-691-91) |
Product NDC | 12634-691 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | DIETHYLPROPION HYDROCHLORIDE ER |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20081023 |
Marketing Category Name | ANDA |
Labeler Name | Apotheca Inc |
Substance Name | DIETHYLPROPION HYDROCHLORIDE |
Strength Number | 75 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Appetite Suppression [PE],Increased Sympathetic Activity [PE],Sympathomimetic Amine Anorectic [EPC] |