ibuprofen - 37808-255-10 - (Ibuprofen)

Alphabetical Index


Drug Information of ibuprofen

Product NDC: 37808-255
Proprietary Name: ibuprofen
Non Proprietary Name: Ibuprofen
Active Ingredient(s): 50    mg/1.25mL & nbsp;   Ibuprofen
Administration Route(s): ORAL
Dosage Form(s): SUSPENSION/ DROPS
Coding System: National Drug Codes(NDC)

Labeler Information of ibuprofen

Product NDC: 37808-255
Labeler Name: H E B
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA075217
Marketing Category: ANDA
Start Marketing Date: 20050225

Package Information of ibuprofen

Package NDC: 37808-255-10
Package Description: 1 BOTTLE in 1 CARTON (37808-255-10) > 30 mL in 1 BOTTLE

NDC Information of ibuprofen

NDC Code 37808-255-10
Proprietary Name ibuprofen
Package Description 1 BOTTLE in 1 CARTON (37808-255-10) > 30 mL in 1 BOTTLE
Product NDC 37808-255
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Ibuprofen
Dosage Form Name SUSPENSION/ DROPS
Route Name ORAL
Start Marketing Date 20050225
Marketing Category Name ANDA
Labeler Name H E B
Substance Name IBUPROFEN
Strength Number 50
Strength Unit mg/1.25mL
Pharmaceutical Classes

Complete Information of ibuprofen


General Information