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Phendimetrazine Tartrate - 21695-597-42 - (Phendimetrazine Tartrate)

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Drug Information of Phendimetrazine Tartrate

Product NDC: 21695-597
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: 21695-597
Labeler Name: Rebel Distributors Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA085588
Marketing Category: ANDA
Start Marketing Date: 20090601

Package Information of Phendimetrazine Tartrate

Package NDC: 21695-597-42
Package Description: 42 TABLET in 1 BOTTLE (21695-597-42)

NDC Information of Phendimetrazine Tartrate

NDC Code 21695-597-42
Proprietary Name Phendimetrazine Tartrate
Package Description 42 TABLET in 1 BOTTLE (21695-597-42)
Product NDC 21695-597
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Phendimetrazine Tartrate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20090601
Marketing Category Name ANDA
Labeler Name Rebel Distributors Corp
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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