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pain relief - 56062-484-78 - (Acetaminophen)

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Drug Information of pain relief

Product NDC: 56062-484
Proprietary Name: pain relief
Non Proprietary Name: Acetaminophen
Active Ingredient(s): 500    mg/1 & nbsp;   Acetaminophen
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of pain relief

Product NDC: 56062-484
Labeler Name: Publix Super Markets Inc
Product Type: HUMAN OTC DRUG
FDA Application Number: part343
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 19880915

Package Information of pain relief

Package NDC: 56062-484-78
Package Description: 1 BOTTLE in 1 CARTON (56062-484-78) > 100 TABLET in 1 BOTTLE

NDC Information of pain relief

NDC Code 56062-484-78
Proprietary Name pain relief
Package Description 1 BOTTLE in 1 CARTON (56062-484-78) > 100 TABLET in 1 BOTTLE
Product NDC 56062-484
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19880915
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Publix Super Markets Inc
Substance Name ACETAMINOPHEN
Strength Number 500
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of pain relief


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