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Phentermine Hydrochloride - 43063-437-98 - (Phentermine Hydrochloride)

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Drug Information of Phentermine Hydrochloride

Product NDC: 43063-437
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: 43063-437
Labeler Name: PD-Rx Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA200272
Marketing Category: ANDA
Start Marketing Date: 20110308

Package Information of Phentermine Hydrochloride

Package NDC: 43063-437-98
Package Description: 120 TABLET in 1 BOTTLE, PLASTIC (43063-437-98)

NDC Information of Phentermine Hydrochloride

NDC Code 43063-437-98
Proprietary Name Phentermine Hydrochloride
Package Description 120 TABLET in 1 BOTTLE, PLASTIC (43063-437-98)
Product NDC 43063-437
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Phentermine Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110308
Marketing Category Name ANDA
Labeler Name PD-Rx Pharmaceuticals, Inc.
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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