Ibuprofen - 0472-1270-94 - (Ibuprofen)

Alphabetical Index


Drug Information of Ibuprofen

Product NDC: 0472-1270
Proprietary Name: Ibuprofen
Non Proprietary Name: Ibuprofen
Active Ingredient(s): 100    mg/5mL & nbsp;   Ibuprofen
Administration Route(s): ORAL
Dosage Form(s): SUSPENSION
Coding System: National Drug Codes(NDC)

Labeler Information of Ibuprofen

Product NDC: 0472-1270
Labeler Name: Actavis Mid Atlantic LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074978
Marketing Category: ANDA
Start Marketing Date: 20020927

Package Information of Ibuprofen

Package NDC: 0472-1270-94
Package Description: 1 BOTTLE in 1 CARTON (0472-1270-94) > 118 mL in 1 BOTTLE

NDC Information of Ibuprofen

NDC Code 0472-1270-94
Proprietary Name Ibuprofen
Package Description 1 BOTTLE in 1 CARTON (0472-1270-94) > 118 mL in 1 BOTTLE
Product NDC 0472-1270
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ibuprofen
Dosage Form Name SUSPENSION
Route Name ORAL
Start Marketing Date 20020927
Marketing Category Name ANDA
Labeler Name Actavis Mid Atlantic LLC
Substance Name IBUPROFEN
Strength Number 100
Strength Unit mg/5mL
Pharmaceutical Classes Cyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC]

Complete Information of Ibuprofen


General Information