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Phendimetrazine Tartrate - 52959-282-35 - (Phendimetrazine Tartrate)

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Drug Information of Phendimetrazine Tartrate

Product NDC: 52959-282
Proprietary Name: Phendimetrazine Tartrate
Non Proprietary Name: Phendimetrazine Tartrate
Active Ingredient(s): 35    mg/1 & nbsp;   Phendimetrazine Tartrate
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Phendimetrazine Tartrate

Product NDC: 52959-282
Labeler Name: H.J. Harkins Company, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA091042
Marketing Category: ANDA
Start Marketing Date: 20100915

Package Information of Phendimetrazine Tartrate

Package NDC: 52959-282-35
Package Description: 35 TABLET in 1 BOTTLE (52959-282-35)

NDC Information of Phendimetrazine Tartrate

NDC Code 52959-282-35
Proprietary Name Phendimetrazine Tartrate
Package Description 35 TABLET in 1 BOTTLE (52959-282-35)
Product NDC 52959-282
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Phendimetrazine Tartrate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20100915
Marketing Category Name ANDA
Labeler Name H.J. Harkins Company, Inc.
Substance Name PHENDIMETRAZINE TARTRATE
Strength Number 35
Strength Unit mg/1
Pharmaceutical Classes Appetite Suppression [PE],Increased Sympathetic Activity [PE],Sympathomimetic Amine Anorectic [EPC]

Complete Information of Phendimetrazine Tartrate


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