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Phendimetrazine Tartrate - 10702-077-10 - (Phendimetrazine Tartrate)

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Drug Information of Phendimetrazine Tartrate

Product NDC: 10702-077
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: 10702-077
Labeler Name: KVK-TECH, INC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA091042
Marketing Category: ANDA
Start Marketing Date: 20100915

Package Information of Phendimetrazine Tartrate

Package NDC: 10702-077-10
Package Description: 1000 TABLET in 1 BOTTLE (10702-077-10)

NDC Information of Phendimetrazine Tartrate

NDC Code 10702-077-10
Proprietary Name Phendimetrazine Tartrate
Package Description 1000 TABLET in 1 BOTTLE (10702-077-10)
Product NDC 10702-077
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 KVK-TECH, 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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