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ADVIL CONGESTION RELIEF - 0573-0195-50 - (IBUPROFEN and PHENYLEPHRINE HYDROCHLORIDE)

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Drug Information of ADVIL CONGESTION RELIEF

Product NDC: 0573-0195
Proprietary Name: ADVIL CONGESTION RELIEF
Non Proprietary Name: IBUPROFEN and PHENYLEPHRINE HYDROCHLORIDE
Active Ingredient(s): 200; 10    mg/1; mg/1 & nbsp;   IBUPROFEN and PHENYLEPHRINE HYDROCHLORIDE
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of ADVIL CONGESTION RELIEF

Product NDC: 0573-0195
Labeler Name: Pfizer Consumer Healthcare
Product Type: HUMAN OTC DRUG
FDA Application Number: NDA022565
Marketing Category: NDA
Start Marketing Date: 20101004

Package Information of ADVIL CONGESTION RELIEF

Package NDC: 0573-0195-50
Package Description: 20 CARTON in 1 TRAY (0573-0195-50) > 5 BLISTER PACK in 1 CARTON > 10 TABLET, FILM COATED in 1 BLISTER PACK

NDC Information of ADVIL CONGESTION RELIEF

NDC Code 0573-0195-50
Proprietary Name ADVIL CONGESTION RELIEF
Package Description 20 CARTON in 1 TRAY (0573-0195-50) > 5 BLISTER PACK in 1 CARTON > 10 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC 0573-0195
Product Type Name HUMAN OTC DRUG
Non Proprietary Name IBUPROFEN and PHENYLEPHRINE HYDROCHLORIDE
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20101004
Marketing Category Name NDA
Labeler Name Pfizer Consumer Healthcare
Substance Name IBUPROFEN; PHENYLEPHRINE HYDROCHLORIDE
Strength Number 200; 10
Strength Unit mg/1; mg/1
Pharmaceutical Classes

Complete Information of ADVIL CONGESTION RELIEF


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