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leader ibuprofen pm - 37205-672-60 - (Diphenhydramine citrate, Ibuprofen)

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Drug Information of leader ibuprofen pm

Product NDC: 37205-672
Proprietary Name: leader ibuprofen pm
Non Proprietary Name: Diphenhydramine citrate, Ibuprofen
Active Ingredient(s): 38; 200    mg/1; mg/1 & nbsp;   Diphenhydramine citrate, Ibuprofen
Administration Route(s): ORAL
Dosage Form(s): TABLET, COATED
Coding System: National Drug Codes(NDC)

Labeler Information of leader ibuprofen pm

Product NDC: 37205-672
Labeler Name: Cardinal Health
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA079113
Marketing Category: ANDA
Start Marketing Date: 20120613

Package Information of leader ibuprofen pm

Package NDC: 37205-672-60
Package Description: 1 BOTTLE in 1 CARTON (37205-672-60) > 20 TABLET, COATED in 1 BOTTLE

NDC Information of leader ibuprofen pm

NDC Code 37205-672-60
Proprietary Name leader ibuprofen pm
Package Description 1 BOTTLE in 1 CARTON (37205-672-60) > 20 TABLET, COATED in 1 BOTTLE
Product NDC 37205-672
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Diphenhydramine citrate, Ibuprofen
Dosage Form Name TABLET, COATED
Route Name ORAL
Start Marketing Date 20120613
Marketing Category Name ANDA
Labeler Name Cardinal Health
Substance Name DIPHENHYDRAMINE CITRATE; IBUPROFEN
Strength Number 38; 200
Strength Unit mg/1; mg/1
Pharmaceutical Classes

Complete Information of leader ibuprofen pm


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