Product NDC: | 54569-2059 |
Proprietary Name: | Diethylpropion HCl Immediate-Release |
Non Proprietary Name: | Diethylpropion hydrochloride |
Active Ingredient(s): | 25 mg/1 & nbsp; Diethylpropion hydrochloride |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 54569-2059 |
Labeler Name: | A-S Medication Solutions LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA011722 |
Marketing Category: | NDA |
Start Marketing Date: | 19590806 |
Package NDC: | 54569-2059-4 |
Package Description: | 28 TABLET in 1 BOTTLE (54569-2059-4) |
NDC Code | 54569-2059-4 |
Proprietary Name | Diethylpropion HCl Immediate-Release |
Package Description | 28 TABLET in 1 BOTTLE (54569-2059-4) |
Product NDC | 54569-2059 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Diethylpropion hydrochloride |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 19590806 |
Marketing Category Name | NDA |
Labeler Name | A-S Medication Solutions LLC |
Substance Name | DIETHYLPROPION HYDROCHLORIDE |
Strength Number | 25 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Appetite Suppression [PE],Increased Sympathetic Activity [PE],Sympathomimetic Amine Anorectic [EPC] |