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Nateglinide - 0591-3354-30 - (Nateglinide)

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Drug Information of Nateglinide

Product NDC: 0591-3354
Proprietary Name: Nateglinide
Non Proprietary Name: Nateglinide
Active Ingredient(s): 60    mg/1 & nbsp;   Nateglinide
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Nateglinide

Product NDC: 0591-3354
Labeler Name: Watson Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077462
Marketing Category: ANDA
Start Marketing Date: 20110330

Package Information of Nateglinide

Package NDC: 0591-3354-30
Package Description: 30 TABLET in 1 BOTTLE, PLASTIC (0591-3354-30)

NDC Information of Nateglinide

NDC Code 0591-3354-30
Proprietary Name Nateglinide
Package Description 30 TABLET in 1 BOTTLE, PLASTIC (0591-3354-30)
Product NDC 0591-3354
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Nateglinide
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110330
Marketing Category Name ANDA
Labeler Name Watson Laboratories, Inc.
Substance Name NATEGLINIDE
Strength Number 60
Strength Unit mg/1
Pharmaceutical Classes Glinide [EPC],Potassium Channel Antagonists [MoA]

Complete Information of Nateglinide


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