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Phentermine Hydrochloride - 10544-099-21 - (Phentermine Hydrochloride)

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Drug Information of Phentermine Hydrochloride

Product NDC: 10544-099
Proprietary Name: Phentermine Hydrochloride
Non Proprietary Name: Phentermine Hydrochloride
Active Ingredient(s): 15    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: 10544-099
Labeler Name: Blenheim Pharmacal, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040886
Marketing Category: ANDA
Start Marketing Date: 20130318

Package Information of Phentermine Hydrochloride

Package NDC: 10544-099-21
Package Description: 21 CAPSULE in 1 BOTTLE (10544-099-21)

NDC Information of Phentermine Hydrochloride

NDC Code 10544-099-21
Proprietary Name Phentermine Hydrochloride
Package Description 21 CAPSULE in 1 BOTTLE (10544-099-21)
Product NDC 10544-099
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Phentermine Hydrochloride
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20130318
Marketing Category Name ANDA
Labeler Name Blenheim Pharmacal, Inc.
Substance Name PHENTERMINE HYDROCHLORIDE
Strength Number 15
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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