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PHENTERMINE HYDROCHLORIDE - 54868-0192-4 - (phentermine hydrochloride)

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Drug Information of PHENTERMINE HYDROCHLORIDE

Product NDC: 54868-0192
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: 54868-0192
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA087022
Marketing Category: ANDA
Start Marketing Date: 19950201

Package Information of PHENTERMINE HYDROCHLORIDE

Package NDC: 54868-0192-4
Package Description: 30 CAPSULE in 1 BOTTLE, PLASTIC (54868-0192-4)

NDC Information of PHENTERMINE HYDROCHLORIDE

NDC Code 54868-0192-4
Proprietary Name PHENTERMINE HYDROCHLORIDE
Package Description 30 CAPSULE in 1 BOTTLE, PLASTIC (54868-0192-4)
Product NDC 54868-0192
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name phentermine hydrochloride
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 19950201
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
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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