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Nateglinide - 55111-329-78 - (Nateglinide)

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Drug Information of Nateglinide

Product NDC: 55111-329
Proprietary Name: Nateglinide
Non Proprietary Name: Nateglinide
Active Ingredient(s): 120    mg/1 & nbsp;   Nateglinide
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Nateglinide

Product NDC: 55111-329
Labeler Name: Dr. Reddy's Laboratories Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077461
Marketing Category: ANDA
Start Marketing Date: 20090909

Package Information of Nateglinide

Package NDC: 55111-329-78
Package Description: 10 BLISTER PACK in 1 CARTON (55111-329-78) > 10 TABLET in 1 BLISTER PACK (55111-329-79)

NDC Information of Nateglinide

NDC Code 55111-329-78
Proprietary Name Nateglinide
Package Description 10 BLISTER PACK in 1 CARTON (55111-329-78) > 10 TABLET in 1 BLISTER PACK (55111-329-79)
Product NDC 55111-329
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Nateglinide
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20090909
Marketing Category Name ANDA
Labeler Name Dr. Reddy's Laboratories Limited
Substance Name NATEGLINIDE
Strength Number 120
Strength Unit mg/1
Pharmaceutical Classes Glinide [EPC],Potassium Channel Antagonists [MoA]

Complete Information of Nateglinide


General Information