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Phentermine Hydrochloride - 63629-1584-5 - (Phentermine Hydrochloride)

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Drug Information of Phentermine Hydrochloride

Product NDC: 63629-1584
Proprietary Name: Phentermine Hydrochloride
Non Proprietary Name: Phentermine Hydrochloride
Active Ingredient(s): 37.5    mg/1 & nbsp;   Phentermine Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Phentermine Hydrochloride

Product NDC: 63629-1584
Labeler Name: Bryant Ranch Prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040377
Marketing Category: ANDA
Start Marketing Date: 20020104

Package Information of Phentermine Hydrochloride

Package NDC: 63629-1584-5
Package Description: 14 TABLET in 1 BOTTLE (63629-1584-5)

NDC Information of Phentermine Hydrochloride

NDC Code 63629-1584-5
Proprietary Name Phentermine Hydrochloride
Package Description 14 TABLET in 1 BOTTLE (63629-1584-5)
Product NDC 63629-1584
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Phentermine Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20020104
Marketing Category Name ANDA
Labeler Name Bryant Ranch Prepack
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 Phentermine Hydrochloride


General Information