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Phendimetrazine Tartrate - 63629-3051-6 - (Phendimetrazine Tartrate)

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Drug Information of Phendimetrazine Tartrate

Product NDC: 63629-3051
Proprietary Name: Phendimetrazine Tartrate
Non Proprietary Name: Phendimetrazine Tartrate
Active Ingredient(s): 105    mg/1 & nbsp;   Phendimetrazine Tartrate
Administration Route(s): ORAL
Dosage Form(s): CAPSULE, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Phendimetrazine Tartrate

Product NDC: 63629-3051
Labeler Name: Bryant Ranch Prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA018074
Marketing Category: NDA
Start Marketing Date: 19770906

Package Information of Phendimetrazine Tartrate

Package NDC: 63629-3051-6
Package Description: 7 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (63629-3051-6)

NDC Information of Phendimetrazine Tartrate

NDC Code 63629-3051-6
Proprietary Name Phendimetrazine Tartrate
Package Description 7 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (63629-3051-6)
Product NDC 63629-3051
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Phendimetrazine Tartrate
Dosage Form Name CAPSULE, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 19770906
Marketing Category Name NDA
Labeler Name Bryant Ranch Prepack
Substance Name PHENDIMETRAZINE TARTRATE
Strength Number 105
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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