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Nateglinide - 49884-985-05 - (Nateglinide)

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Drug Information of Nateglinide

Product NDC: 49884-985
Proprietary Name: Nateglinide
Non Proprietary Name: Nateglinide
Active Ingredient(s): 120    mg/1 & nbsp;   Nateglinide
Administration Route(s): ORAL
Dosage Form(s): TABLET, COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Nateglinide

Product NDC: 49884-985
Labeler Name: Par Pharmaceutical Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077463
Marketing Category: ANDA
Start Marketing Date: 20090908

Package Information of Nateglinide

Package NDC: 49884-985-05
Package Description: 500 TABLET, COATED in 1 BOTTLE, PLASTIC (49884-985-05)

NDC Information of Nateglinide

NDC Code 49884-985-05
Proprietary Name Nateglinide
Package Description 500 TABLET, COATED in 1 BOTTLE, PLASTIC (49884-985-05)
Product NDC 49884-985
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Nateglinide
Dosage Form Name TABLET, COATED
Route Name ORAL
Start Marketing Date 20090908
Marketing Category Name ANDA
Labeler Name Par Pharmaceutical Inc.
Substance Name NATEGLINIDE
Strength Number 120
Strength Unit mg/1
Pharmaceutical Classes Glinide [EPC],Potassium Channel Antagonists [MoA]

Complete Information of Nateglinide


General Information