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Suprenza
Suprenza - 24090-721-85 - (phentermine hydrochloride)
Drug Information of Suprenza
| Product NDC: | 24090-721 |
| Proprietary Name: | Suprenza |
| Non Proprietary Name: | phentermine hydrochloride |
| Active Ingredient(s): | 30 mg/1 & nbsp; phentermine hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, ORALLY DISINTEGRATING |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Suprenza
| Product NDC: | 24090-721 |
| Labeler Name: | Akrimax Pharmaceuticals, LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA202088 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20121214 |
Package Information of Suprenza
| Package NDC: | 24090-721-85 |
| Package Description: | 30 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE, PLASTIC (24090-721-85) |
NDC Information of Suprenza
| NDC Code | 24090-721-85 |
| Proprietary Name | Suprenza |
| Package Description | 30 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE, PLASTIC (24090-721-85) |
| Product NDC | 24090-721 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | phentermine hydrochloride |
| Dosage Form Name | TABLET, ORALLY DISINTEGRATING |
| Route Name | ORAL |
| Start Marketing Date | 20121214 |
| Marketing Category Name | NDA |
| Labeler Name | Akrimax Pharmaceuticals, LLC |
| Substance Name | PHENTERMINE HYDROCHLORIDE |
| Strength Number | 30 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Appetite Suppression [PE],Increased Sympathetic Activity [PE],Sympathomimetic Amine Anorectic [EPC] |
