Ibuprofen - 62207-366-43 - (Ibuprofen)

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Drug Information of Ibuprofen

Product NDC: 62207-366
Proprietary Name: 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 Ibuprofen

Product NDC: 62207-366
Labeler Name: Granules India Limited
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA079174
Marketing Category: ANDA
Start Marketing Date: 20110101

Package Information of Ibuprofen

Package NDC: 62207-366-43
Package Description: 100 TABLET in 1 BOTTLE (62207-366-43)

NDC Information of Ibuprofen

NDC Code 62207-366-43
Proprietary Name Ibuprofen
Package Description 100 TABLET in 1 BOTTLE (62207-366-43)
Product NDC 62207-366
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Ibuprofen
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110101
Marketing Category Name ANDA
Labeler Name Granules India Limited
Substance Name IBUPROFEN
Strength Number 200
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Ibuprofen


General Information