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Equaline pain relief - 41163-484-02 - (Acetaminophen)

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Drug Information of Equaline pain relief

Product NDC: 41163-484
Proprietary Name: Equaline 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 Equaline pain relief

Product NDC: 41163-484
Labeler Name: Supervalu Inc
Product Type: HUMAN OTC DRUG
FDA Application Number: part343
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20040818

Package Information of Equaline pain relief

Package NDC: 41163-484-02
Package Description: 550 TABLET in 1 BOTTLE (41163-484-02)

NDC Information of Equaline pain relief

NDC Code 41163-484-02
Proprietary Name Equaline pain relief
Package Description 550 TABLET in 1 BOTTLE (41163-484-02)
Product NDC 41163-484
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20040818
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Supervalu Inc
Substance Name ACETAMINOPHEN
Strength Number 500
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Equaline pain relief


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