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phendimetrazine tartrate - 43547-264-11 - (phendimetrazine tartrate)

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Drug Information of phendimetrazine tartrate

Product NDC: 43547-264
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: 43547-264
Labeler Name: Solco Healthcare US LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA089452
Marketing Category: ANDA
Start Marketing Date: 20110801

Package Information of phendimetrazine tartrate

Package NDC: 43547-264-11
Package Description: 1000 TABLET in 1 BOTTLE, PLASTIC (43547-264-11)

NDC Information of phendimetrazine tartrate

NDC Code 43547-264-11
Proprietary Name phendimetrazine tartrate
Package Description 1000 TABLET in 1 BOTTLE, PLASTIC (43547-264-11)
Product NDC 43547-264
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name phendimetrazine tartrate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110801
Marketing Category Name ANDA
Labeler Name Solco Healthcare US LLC
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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