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Film Coated Ibuprofen - 64092-200-30 - (Ibuprofen)

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Drug Information of Film Coated Ibuprofen

Product NDC: 64092-200
Proprietary Name: Film Coated Ibuprofen
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 Film Coated Ibuprofen

Product NDC: 64092-200
Labeler Name: GREAT LAKES WHOLESALE, MARKETING, & SALES, INC.
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA075010
Marketing Category: ANDA
Start Marketing Date: 19880524

Package Information of Film Coated Ibuprofen

Package NDC: 64092-200-30
Package Description: 1 BOTTLE in 1 CARTON (64092-200-30) > 30 TABLET in 1 BOTTLE

NDC Information of Film Coated Ibuprofen

NDC Code 64092-200-30
Proprietary Name Film Coated Ibuprofen
Package Description 1 BOTTLE in 1 CARTON (64092-200-30) > 30 TABLET in 1 BOTTLE
Product NDC 64092-200
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Ibuprofen
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19880524
Marketing Category Name ANDA
Labeler Name GREAT LAKES WHOLESALE, MARKETING, & SALES, INC.
Substance Name IBUPROFEN
Strength Number 200
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Film Coated Ibuprofen


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