Ibuprofen - 66689-009-50 - (Ibuprofen)

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Drug Information of Ibuprofen

Product NDC: 66689-009
Proprietary Name: Ibuprofen
Non Proprietary Name: Ibuprofen
Active Ingredient(s): 100    mg/5mL & nbsp;   Ibuprofen
Administration Route(s): ORAL
Dosage Form(s): SUSPENSION
Coding System: National Drug Codes(NDC)

Labeler Information of Ibuprofen

Product NDC: 66689-009
Labeler Name: VistaPharm, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074978
Marketing Category: ANDA
Start Marketing Date: 20120816

Package Information of Ibuprofen

Package NDC: 66689-009-50
Package Description: 5 TRAY in 1 CASE (66689-009-50) > 10 CUP, UNIT-DOSE in 1 TRAY > 5 mL in 1 CUP, UNIT-DOSE (66689-009-01)

NDC Information of Ibuprofen

NDC Code 66689-009-50
Proprietary Name Ibuprofen
Package Description 5 TRAY in 1 CASE (66689-009-50) > 10 CUP, UNIT-DOSE in 1 TRAY > 5 mL in 1 CUP, UNIT-DOSE (66689-009-01)
Product NDC 66689-009
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ibuprofen
Dosage Form Name SUSPENSION
Route Name ORAL
Start Marketing Date 20120816
Marketing Category Name ANDA
Labeler Name VistaPharm, Inc.
Substance Name IBUPROFEN
Strength Number 100
Strength Unit mg/5mL
Pharmaceutical Classes Cyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC]

Complete Information of Ibuprofen


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