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Phentermine Hydrochloride - 50436-6744-2 - (Phentermine Hydrochloride)

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Drug Information of Phentermine Hydrochloride

Product NDC: 50436-6744
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: 50436-6744
Labeler Name: Unit Dose Services
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040555
Marketing Category: ANDA
Start Marketing Date: 20050415

Package Information of Phentermine Hydrochloride

Package NDC: 50436-6744-2
Package Description: 7 TABLET in 1 BOTTLE (50436-6744-2)

NDC Information of Phentermine Hydrochloride

NDC Code 50436-6744-2
Proprietary Name Phentermine Hydrochloride
Package Description 7 TABLET in 1 BOTTLE (50436-6744-2)
Product NDC 50436-6744
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Phentermine Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20050415
Marketing Category Name ANDA
Labeler Name Unit Dose Services
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


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