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Childrens Ibuprofen - 68094-494-61 - (Ibuprofen)

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Drug Information of Childrens Ibuprofen

Product NDC: 68094-494
Proprietary Name: Childrens 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 Childrens Ibuprofen

Product NDC: 68094-494
Labeler Name: Precision Dose Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA074937
Marketing Category: ANDA
Start Marketing Date: 20040413

Package Information of Childrens Ibuprofen

Package NDC: 68094-494-61
Package Description: 10 TRAY in 1 CASE (68094-494-61) > 10 CUP, UNIT-DOSE in 1 TRAY > 5 mL in 1 CUP, UNIT-DOSE (68094-494-59)

NDC Information of Childrens Ibuprofen

NDC Code 68094-494-61
Proprietary Name Childrens Ibuprofen
Package Description 10 TRAY in 1 CASE (68094-494-61) > 10 CUP, UNIT-DOSE in 1 TRAY > 5 mL in 1 CUP, UNIT-DOSE (68094-494-59)
Product NDC 68094-494
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Ibuprofen
Dosage Form Name SUSPENSION
Route Name ORAL
Start Marketing Date 20040413
Marketing Category Name ANDA
Labeler Name Precision Dose Inc.
Substance Name IBUPROFEN
Strength Number 100
Strength Unit mg/5mL
Pharmaceutical Classes

Complete Information of Childrens Ibuprofen


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