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Acetaminophen - 57344-004-08 - (Acetaminophen)

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Drug Information of Acetaminophen

Product NDC: 57344-004
Proprietary Name: Acetaminophen
Non Proprietary Name: Acetaminophen
Active Ingredient(s): 500    mg/1 & nbsp;   Acetaminophen
Administration Route(s): ORAL
Dosage Form(s): TABLET, COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Acetaminophen

Product NDC: 57344-004
Labeler Name: AAA Pharmaceutical, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part343
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20121213

Package Information of Acetaminophen

Package NDC: 57344-004-08
Package Description: 150 TABLET, COATED in 1 BOTTLE, PLASTIC (57344-004-08)

NDC Information of Acetaminophen

NDC Code 57344-004-08
Proprietary Name Acetaminophen
Package Description 150 TABLET, COATED in 1 BOTTLE, PLASTIC (57344-004-08)
Product NDC 57344-004
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen
Dosage Form Name TABLET, COATED
Route Name ORAL
Start Marketing Date 20121213
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name AAA Pharmaceutical, Inc.
Substance Name ACETAMINOPHEN
Strength Number 500
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Acetaminophen


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