Home > National Drug Code (NDC) > arthritis pain reliever

arthritis pain reliever - 0363-0544-85 - (Acetaminophen)

Alphabetical Index


Drug Information of arthritis pain reliever

Product NDC: 0363-0544
Proprietary Name: arthritis pain reliever
Non Proprietary Name: Acetaminophen
Active Ingredient(s): 650    mg/1 & nbsp;   Acetaminophen
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of arthritis pain reliever

Product NDC: 0363-0544
Labeler Name: Walgreen Company
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA075077
Marketing Category: ANDA
Start Marketing Date: 20000526

Package Information of arthritis pain reliever

Package NDC: 0363-0544-85
Package Description: 1 BOTTLE in 1 CARTON (0363-0544-85) > 250 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE

NDC Information of arthritis pain reliever

NDC Code 0363-0544-85
Proprietary Name arthritis pain reliever
Package Description 1 BOTTLE in 1 CARTON (0363-0544-85) > 250 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE
Product NDC 0363-0544
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen
Dosage Form Name TABLET, FILM COATED, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20000526
Marketing Category Name ANDA
Labeler Name Walgreen Company
Substance Name ACETAMINOPHEN
Strength Number 650
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of arthritis pain reliever


General Information