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Diethylpropion HCl Immediate-Release
Diethylpropion HCl Immediate-Release - 68387-695-21 - (Diethylpropion hydrochloride)
Drug Information of Diethylpropion HCl Immediate-Release
| Product NDC: | 68387-695 |
| 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) |
Labeler Information of Diethylpropion HCl Immediate-Release
| Product NDC: | 68387-695 |
| Labeler Name: | Keltman Pharmaceuticals Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA011722 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20100607 |
Package Information of Diethylpropion HCl Immediate-Release
| Package NDC: | 68387-695-21 |
| Package Description: | 21 TABLET in 1 BOTTLE, PLASTIC (68387-695-21) |
NDC Information of Diethylpropion HCl Immediate-Release
| NDC Code | 68387-695-21 |
| Proprietary Name | Diethylpropion HCl Immediate-Release |
| Package Description | 21 TABLET in 1 BOTTLE, PLASTIC (68387-695-21) |
| Product NDC | 68387-695 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Diethylpropion hydrochloride |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20100607 |
| Marketing Category Name | ANDA |
| Labeler Name | Keltman Pharmaceuticals Inc. |
| Substance Name | DIETHYLPROPION HYDROCHLORIDE |
| Strength Number | 25 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Appetite Suppression [PE],Increased Sympathetic Activity [PE],Sympathomimetic Amine Anorectic [EPC] |
