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Phentermine Hydrochloride - 54569-0392-3 - (Phentermine Hydrochloride)

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Drug Information of Phentermine Hydrochloride

Product NDC: 54569-0392
Proprietary Name: Phentermine Hydrochloride
Non Proprietary Name: Phentermine Hydrochloride
Active Ingredient(s): 30    mg/1 & nbsp;   Phentermine Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Phentermine Hydrochloride

Product NDC: 54569-0392
Labeler Name: A-S Medication Solutions LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040886
Marketing Category: ANDA
Start Marketing Date: 20120807

Package Information of Phentermine Hydrochloride

Package NDC: 54569-0392-3
Package Description: 7 CAPSULE in 1 BOTTLE (54569-0392-3)

NDC Information of Phentermine Hydrochloride

NDC Code 54569-0392-3
Proprietary Name Phentermine Hydrochloride
Package Description 7 CAPSULE in 1 BOTTLE (54569-0392-3)
Product NDC 54569-0392
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Phentermine Hydrochloride
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20120807
Marketing Category Name ANDA
Labeler Name A-S Medication Solutions 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]

Complete Information of Phentermine Hydrochloride


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