ADVIL PM - 0573-0164-41 - (DIPHENHYDRAMINE CITRATE and IBUPROFEN)

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Drug Information of ADVIL PM

Product NDC: 0573-0164
Proprietary Name: ADVIL PM
Non Proprietary Name: DIPHENHYDRAMINE CITRATE and IBUPROFEN
Active Ingredient(s): 38; 200    mg/1; mg/1 & nbsp;   DIPHENHYDRAMINE CITRATE and IBUPROFEN
Administration Route(s): ORAL
Dosage Form(s): TABLET, COATED
Coding System: National Drug Codes(NDC)

Labeler Information of ADVIL PM

Product NDC: 0573-0164
Labeler Name: Pfizer Consumer Healthcare
Product Type: HUMAN OTC DRUG
FDA Application Number: NDA021394
Marketing Category: NDA
Start Marketing Date: 20051221

Package Information of ADVIL PM

Package NDC: 0573-0164-41
Package Description: 1 BOTTLE in 1 CARTON (0573-0164-41) > 100 TABLET, COATED in 1 BOTTLE

NDC Information of ADVIL PM

NDC Code 0573-0164-41
Proprietary Name ADVIL PM
Package Description 1 BOTTLE in 1 CARTON (0573-0164-41) > 100 TABLET, COATED in 1 BOTTLE
Product NDC 0573-0164
Product Type Name HUMAN OTC DRUG
Non Proprietary Name DIPHENHYDRAMINE CITRATE and IBUPROFEN
Dosage Form Name TABLET, COATED
Route Name ORAL
Start Marketing Date 20051221
Marketing Category Name NDA
Labeler Name Pfizer Consumer Healthcare
Substance Name DIPHENHYDRAMINE CITRATE; IBUPROFEN
Strength Number 38; 200
Strength Unit mg/1; mg/1
Pharmaceutical Classes

Complete Information of ADVIL PM


General Information