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Acetaminophen - 41163-104-12 - (Acetaminophen)

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Drug Information of Acetaminophen

Product NDC: 41163-104
Proprietary Name: Acetaminophen
Non Proprietary Name: Acetaminophen
Active Ingredient(s): 325    mg/1 & nbsp;   Acetaminophen
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Acetaminophen

Product NDC: 41163-104
Labeler Name: SUPERVALU INC.
Product Type: HUMAN OTC DRUG
FDA Application Number: part343
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 19900713

Package Information of Acetaminophen

Package NDC: 41163-104-12
Package Description: 1 BOTTLE in 1 CARTON (41163-104-12) > 100 TABLET in 1 BOTTLE

NDC Information of Acetaminophen

NDC Code 41163-104-12
Proprietary Name Acetaminophen
Package Description 1 BOTTLE in 1 CARTON (41163-104-12) > 100 TABLET in 1 BOTTLE
Product NDC 41163-104
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19900713
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name SUPERVALU INC.
Substance Name ACETAMINOPHEN
Strength Number 325
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Acetaminophen


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