Ibuprofen - 49999-071-30 - (Ibuprofen)

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Drug Information of Ibuprofen

Product NDC: 49999-071
Proprietary Name: Ibuprofen
Non Proprietary Name: Ibuprofen
Active Ingredient(s): 200    mg/1 & nbsp;   Ibuprofen
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Ibuprofen

Product NDC: 49999-071
Labeler Name: Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
Product Type: HUMAN OTC DRUG
FDA Application Number: part343
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20120216

Package Information of Ibuprofen

Package NDC: 49999-071-30
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE (49999-071-30)

NDC Information of Ibuprofen

NDC Code 49999-071-30
Proprietary Name Ibuprofen
Package Description 30 TABLET, FILM COATED in 1 BOTTLE (49999-071-30)
Product NDC 49999-071
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Ibuprofen
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20120216
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
Substance Name IBUPROFEN
Strength Number 200
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Ibuprofen


General Information