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Acetaminophen - 54868-0548-4 - (Acetaminophen)

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Drug Information of Acetaminophen

Product NDC: 54868-0548
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: 54868-0548
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part343
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20021024

Package Information of Acetaminophen

Package NDC: 54868-0548-4
Package Description: 100 TABLET in 1 BOTTLE (54868-0548-4)

NDC Information of Acetaminophen

NDC Code 54868-0548-4
Proprietary Name Acetaminophen
Package Description 100 TABLET in 1 BOTTLE (54868-0548-4)
Product NDC 54868-0548
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20021024
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Physicians Total Care, Inc.
Strength Number 325
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Acetaminophen

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