Home > National Drug Code (NDC) > Ibuprofen PM

Ibuprofen PM - 50844-732-21 - (Ibuprofen and Diphenhydramine HCl)

Alphabetical Index


Drug Information of Ibuprofen PM

Product NDC: 50844-732
Proprietary Name: Ibuprofen PM
Non Proprietary Name: Ibuprofen and Diphenhydramine HCl
Active Ingredient(s): 25; 200    mg/1; mg/1 & nbsp;   Ibuprofen and Diphenhydramine HCl
Administration Route(s): ORAL
Dosage Form(s): CAPSULE, LIQUID FILLED
Coding System: National Drug Codes(NDC)

Labeler Information of Ibuprofen PM

Product NDC: 50844-732
Labeler Name: LNK International, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA200888
Marketing Category: ANDA
Start Marketing Date: 20120305

Package Information of Ibuprofen PM

Package NDC: 50844-732-21
Package Description: 2 BLISTER PACK in 1 CARTON (50844-732-21) > 8 CAPSULE, LIQUID FILLED in 1 BLISTER PACK

NDC Information of Ibuprofen PM

NDC Code 50844-732-21
Proprietary Name Ibuprofen PM
Package Description 2 BLISTER PACK in 1 CARTON (50844-732-21) > 8 CAPSULE, LIQUID FILLED in 1 BLISTER PACK
Product NDC 50844-732
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Ibuprofen and Diphenhydramine HCl
Dosage Form Name CAPSULE, LIQUID FILLED
Route Name ORAL
Start Marketing Date 20120305
Marketing Category Name ANDA
Labeler Name LNK International, Inc.
Substance Name DIPHENHYDRAMINE HYDROCHLORIDE; IBUPROFEN
Strength Number 25; 200
Strength Unit mg/1; mg/1
Pharmaceutical Classes

Complete Information of Ibuprofen PM


General Information