Ibuprofen - 49035-393-12 - (Ibuprofen)

Alphabetical Index


Drug Information of Ibuprofen

Product NDC: 49035-393
Proprietary Name: Ibuprofen
Non Proprietary Name: Ibuprofen
Active Ingredient(s): 200    mg/1 & nbsp;   Ibuprofen
Administration Route(s): ORAL
Dosage Form(s): CAPSULE, COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Ibuprofen

Product NDC: 49035-393
Labeler Name: Wal-Mart Stores Inc
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA075139
Marketing Category: ANDA
Start Marketing Date: 20020408

Package Information of Ibuprofen

Package NDC: 49035-393-12
Package Description: 2 BOTTLE in 1 CARTON (49035-393-12) > 100 CAPSULE, COATED in 1 BOTTLE

NDC Information of Ibuprofen

NDC Code 49035-393-12
Proprietary Name Ibuprofen
Package Description 2 BOTTLE in 1 CARTON (49035-393-12) > 100 CAPSULE, COATED in 1 BOTTLE
Product NDC 49035-393
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Ibuprofen
Dosage Form Name CAPSULE, COATED
Route Name ORAL
Start Marketing Date 20020408
Marketing Category Name ANDA
Labeler Name Wal-Mart Stores Inc
Substance Name IBUPROFEN
Strength Number 200
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Ibuprofen


General Information