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Ibuprofen IB - 55319-393-12 - (Ibuprofen)

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Drug Information of Ibuprofen IB

Product NDC: 55319-393
Proprietary Name: Ibuprofen IB
Non Proprietary Name: Ibuprofen
Active Ingredient(s): 200    mg/1 & nbsp;   Ibuprofen
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Ibuprofen IB

Product NDC: 55319-393
Labeler Name: Family Dollar
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA075139
Marketing Category: ANDA
Start Marketing Date: 20020408

Package Information of Ibuprofen IB

Package NDC: 55319-393-12
Package Description: 1 BOTTLE, PLASTIC in 1 CARTON (55319-393-12) > 100 TABLET in 1 BOTTLE, PLASTIC

NDC Information of Ibuprofen IB

NDC Code 55319-393-12
Proprietary Name Ibuprofen IB
Package Description 1 BOTTLE, PLASTIC in 1 CARTON (55319-393-12) > 100 TABLET in 1 BOTTLE, PLASTIC
Product NDC 55319-393
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Ibuprofen
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20020408
Marketing Category Name ANDA
Labeler Name Family Dollar
Substance Name IBUPROFEN
Strength Number 200
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Ibuprofen IB


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