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arthritis pain relief - 56062-544-78 - (Acetaminophen)

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Drug Information of arthritis pain relief

Product NDC: 56062-544
Proprietary Name: arthritis pain relief
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 relief

Product NDC: 56062-544
Labeler Name: Publix Super Markets Inc
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA075077
Marketing Category: ANDA
Start Marketing Date: 20071126

Package Information of arthritis pain relief

Package NDC: 56062-544-78
Package Description: 1 BOTTLE in 1 CARTON (56062-544-78) > 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE

NDC Information of arthritis pain relief

NDC Code 56062-544-78
Proprietary Name arthritis pain relief
Package Description 1 BOTTLE in 1 CARTON (56062-544-78) > 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE
Product NDC 56062-544
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen
Dosage Form Name TABLET, FILM COATED, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20071126
Marketing Category Name ANDA
Labeler Name Publix Super Markets Inc
Substance Name ACETAMINOPHEN
Strength Number 650
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of arthritis pain relief


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