ibuprofen - 37808-604-71 - (Ibuprofen)

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Drug Information of ibuprofen

Product NDC: 37808-604
Proprietary Name: ibuprofen
Non Proprietary Name: Ibuprofen
Active Ingredient(s): 200    mg/1 & nbsp;   Ibuprofen
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of ibuprofen

Product NDC: 37808-604
Labeler Name: H E B
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA072096
Marketing Category: ANDA
Start Marketing Date: 19890215

Package Information of ibuprofen

Package NDC: 37808-604-71
Package Description: 1 BOTTLE in 1 CARTON (37808-604-71) > 50 TABLET, FILM COATED in 1 BOTTLE

NDC Information of ibuprofen

NDC Code 37808-604-71
Proprietary Name ibuprofen
Package Description 1 BOTTLE in 1 CARTON (37808-604-71) > 50 TABLET, FILM COATED in 1 BOTTLE
Product NDC 37808-604
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Ibuprofen
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 19890215
Marketing Category Name ANDA
Labeler Name H E B
Substance Name IBUPROFEN
Strength Number 200
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of ibuprofen


General Information