Ibuprofen - 37808-198-20 - (Ibuprofen)

Alphabetical Index


Drug Information of Ibuprofen

Product NDC: 37808-198
Proprietary Name: Ibuprofen
Non Proprietary Name: Ibuprofen
Active Ingredient(s): 200    mg/1 & nbsp;   Ibuprofen
Administration Route(s): ORAL
Dosage Form(s): CAPSULE, LIQUID FILLED
Coding System: National Drug Codes(NDC)

Labeler Information of Ibuprofen

Product NDC: 37808-198
Labeler Name: H E B
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA078682
Marketing Category: ANDA
Start Marketing Date: 20130108

Package Information of Ibuprofen

Package NDC: 37808-198-20
Package Description: 1 BOTTLE in 1 BOX (37808-198-20) > 20 CAPSULE, LIQUID FILLED in 1 BOTTLE

NDC Information of Ibuprofen

NDC Code 37808-198-20
Proprietary Name Ibuprofen
Package Description 1 BOTTLE in 1 BOX (37808-198-20) > 20 CAPSULE, LIQUID FILLED in 1 BOTTLE
Product NDC 37808-198
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Ibuprofen
Dosage Form Name CAPSULE, LIQUID FILLED
Route Name ORAL
Start Marketing Date 20130108
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