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MEDI-FIRST Ibuprofen - 47682-808-33 - (Ibuprofen)

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Drug Information of MEDI-FIRST Ibuprofen

Product NDC: 47682-808
Proprietary Name: MEDI-FIRST 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 MEDI-FIRST Ibuprofen

Product NDC: 47682-808
Labeler Name: Unifirst First Aid Corporation
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA075139
Marketing Category: ANDA
Start Marketing Date: 20081230

Package Information of MEDI-FIRST Ibuprofen

Package NDC: 47682-808-33
Package Description: 50 PACKET in 1 BOX, UNIT-DOSE (47682-808-33) > 2 TABLET, FILM COATED in 1 PACKET (47682-808-99)

NDC Information of MEDI-FIRST Ibuprofen

NDC Code 47682-808-33
Proprietary Name MEDI-FIRST Ibuprofen
Package Description 50 PACKET in 1 BOX, UNIT-DOSE (47682-808-33) > 2 TABLET, FILM COATED in 1 PACKET (47682-808-99)
Product NDC 47682-808
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Ibuprofen
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20081230
Marketing Category Name ANDA
Labeler Name Unifirst First Aid Corporation
Substance Name IBUPROFEN
Strength Number 200
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of MEDI-FIRST Ibuprofen


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