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Diethylpropion Hydrochloride
Diethylpropion Hydrochloride - 0527-1477-25 - (Diethylpropion Hydrochloride)
Drug Information of Diethylpropion Hydrochloride
| Product NDC: | 0527-1477 |
| Proprietary Name: | Diethylpropion Hydrochloride |
| Non Proprietary Name: | Diethylpropion Hydrochloride |
| Active Ingredient(s): | 75 mg/1 & nbsp; Diethylpropion Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Diethylpropion Hydrochloride
| Product NDC: | 0527-1477 |
| Labeler Name: | Lannett Company, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA091680 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20111024 |
Package Information of Diethylpropion Hydrochloride
| Package NDC: | 0527-1477-25 |
| Package Description: | 250 TABLET, EXTENDED RELEASE in 1 BOTTLE (0527-1477-25) |
NDC Information of Diethylpropion Hydrochloride
| NDC Code | 0527-1477-25 |
| Proprietary Name | Diethylpropion Hydrochloride |
| Package Description | 250 TABLET, EXTENDED RELEASE in 1 BOTTLE (0527-1477-25) |
| Product NDC | 0527-1477 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Diethylpropion Hydrochloride |
| Dosage Form Name | TABLET, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20111024 |
| Marketing Category Name | ANDA |
| Labeler Name | Lannett Company, 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] |
