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Acetaminophen - 54868-5625-0 - (Acetaminophen)

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Drug Information of Acetaminophen

Product NDC: 54868-5625
Proprietary Name: Acetaminophen
Non Proprietary Name: Acetaminophen
Active Ingredient(s): 80    mg/1 & nbsp;   Acetaminophen
Administration Route(s): ORAL
Dosage Form(s): TABLET, CHEWABLE
Coding System: National Drug Codes(NDC)

Labeler Information of Acetaminophen

Product NDC: 54868-5625
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part343
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20060629

Package Information of Acetaminophen

Package NDC: 54868-5625-0
Package Description: 1 BOTTLE, PLASTIC in 1 CARTON (54868-5625-0) > 30 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC

NDC Information of Acetaminophen

NDC Code 54868-5625-0
Proprietary Name Acetaminophen
Package Description 1 BOTTLE, PLASTIC in 1 CARTON (54868-5625-0) > 30 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC
Product NDC 54868-5625
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen
Dosage Form Name TABLET, CHEWABLE
Route Name ORAL
Start Marketing Date 20060629
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Physicians Total Care, Inc.
Substance Name ACETAMINOPHEN
Strength Number 80
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Acetaminophen


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