ibuprofen - 37808-647-78 - (Ibuprofen)

Alphabetical Index


Drug Information of ibuprofen

Product NDC: 37808-647
Proprietary Name: ibuprofen
Non Proprietary Name: Ibuprofen
Active Ingredient(s): 200    mg/1 & nbsp;   Ibuprofen
Administration Route(s): ORAL
Dosage Form(s): TABLET, COATED
Coding System: National Drug Codes(NDC)

Labeler Information of ibuprofen

Product NDC: 37808-647
Labeler Name: H E B
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA072096
Marketing Category: ANDA
Start Marketing Date: 19910809

Package Information of ibuprofen

Package NDC: 37808-647-78
Package Description: 1 BOTTLE in 1 CARTON (37808-647-78) > 100 TABLET, COATED in 1 BOTTLE

NDC Information of ibuprofen

NDC Code 37808-647-78
Proprietary Name ibuprofen
Package Description 1 BOTTLE in 1 CARTON (37808-647-78) > 100 TABLET, COATED in 1 BOTTLE
Product NDC 37808-647
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Ibuprofen
Dosage Form Name TABLET, COATED
Route Name ORAL
Start Marketing Date 19910809
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