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Childrens Ibuprofen - 68788-9109-1 - (Ibuprofen)

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Drug Information of Childrens Ibuprofen

Product NDC: 68788-9109
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: 68788-9109
Labeler Name: Preferred Pharmaceuticals, Inc
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA074916
Marketing Category: ANDA
Start Marketing Date: 20060601

Package Information of Childrens Ibuprofen

Package NDC: 68788-9109-1
Package Description: 1 BOTTLE in 1 CARTON (68788-9109-1) > 118 mL in 1 BOTTLE

NDC Information of Childrens Ibuprofen

NDC Code 68788-9109-1
Proprietary Name Childrens Ibuprofen
Package Description 1 BOTTLE in 1 CARTON (68788-9109-1) > 118 mL in 1 BOTTLE
Product NDC 68788-9109
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Ibuprofen
Dosage Form Name SUSPENSION
Route Name ORAL
Start Marketing Date 20060601
Marketing Category Name ANDA
Labeler Name Preferred Pharmaceuticals, Inc
Substance Name IBUPROFEN
Strength Number 100
Strength Unit mg/5mL
Pharmaceutical Classes

Complete Information of Childrens Ibuprofen


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