Suprenza - 24090-722-88 - (phentermine hydrochloride)

Alphabetical Index


Drug Information of Suprenza

Product NDC: 24090-722
Proprietary Name: Suprenza
Non Proprietary Name: phentermine hydrochloride
Active Ingredient(s): 37.5    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: 24090-722
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: 24090-722-88
Package Description: 100 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE, PLASTIC (24090-722-88)

NDC Information of Suprenza

NDC Code 24090-722-88
Proprietary Name Suprenza
Package Description 100 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE, PLASTIC (24090-722-88)
Product NDC 24090-722
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 37.5
Strength Unit mg/1
Pharmaceutical Classes Appetite Suppression [PE],Increased Sympathetic Activity [PE],Sympathomimetic Amine Anorectic [EPC]

Complete Information of Suprenza


General Information