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Phentermine Hydrochloride - 0527-1742-01 - (Phentermine Hydrochloride)

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Drug Information of Phentermine Hydrochloride

Product NDC: 0527-1742
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: 0527-1742
Labeler Name: Lannett Company, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA087022
Marketing Category: ANDA
Start Marketing Date: 20120120

Package Information of Phentermine Hydrochloride

Package NDC: 0527-1742-01
Package Description: 100 CAPSULE in 1 BOTTLE (0527-1742-01)

NDC Information of Phentermine Hydrochloride

NDC Code 0527-1742-01
Proprietary Name Phentermine Hydrochloride
Package Description 100 CAPSULE in 1 BOTTLE (0527-1742-01)
Product NDC 0527-1742
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Phentermine Hydrochloride
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20120120
Marketing Category Name ANDA
Labeler Name Lannett Company, 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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