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INFANTS ADVIL - 0573-0191-20 - (IBUPROFEN)

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Drug Information of INFANTS ADVIL

Product NDC: 0573-0191
Proprietary Name: INFANTS ADVIL
Non Proprietary Name: IBUPROFEN
Active Ingredient(s): 50    mg/1.25mL & nbsp;   IBUPROFEN
Administration Route(s): ORAL
Dosage Form(s): SUSPENSION/ DROPS
Coding System: National Drug Codes(NDC)

Labeler Information of INFANTS ADVIL

Product NDC: 0573-0191
Labeler Name: Pfizer Consumer Healthcare
Product Type: HUMAN OTC DRUG
FDA Application Number: NDA020812
Marketing Category: NDA
Start Marketing Date: 19980130

Package Information of INFANTS ADVIL

Package NDC: 0573-0191-20
Package Description: 1 BOTTLE, DROPPER in 1 CARTON (0573-0191-20) > 15 mL in 1 BOTTLE, DROPPER

NDC Information of INFANTS ADVIL

NDC Code 0573-0191-20
Proprietary Name INFANTS ADVIL
Package Description 1 BOTTLE, DROPPER in 1 CARTON (0573-0191-20) > 15 mL in 1 BOTTLE, DROPPER
Product NDC 0573-0191
Product Type Name HUMAN OTC DRUG
Non Proprietary Name IBUPROFEN
Dosage Form Name SUSPENSION/ DROPS
Route Name ORAL
Start Marketing Date 19980130
Marketing Category Name NDA
Labeler Name Pfizer Consumer Healthcare
Substance Name IBUPROFEN
Strength Number 50
Strength Unit mg/1.25mL
Pharmaceutical Classes

Complete Information of INFANTS ADVIL


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