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Acetaminophen - 57344-001-07 - (Acetaminophen)

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Drug Information of Acetaminophen

Product NDC: 57344-001
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: 57344-001
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: 57344-001-07
Package Description: 1 BOTTLE, PLASTIC in 1 CARTON (57344-001-07) > 24 TABLET in 1 BOTTLE, PLASTIC

NDC Information of Acetaminophen

NDC Code 57344-001-07
Proprietary Name Acetaminophen
Package Description 1 BOTTLE, PLASTIC in 1 CARTON (57344-001-07) > 24 TABLET in 1 BOTTLE, PLASTIC
Product NDC 57344-001
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20121213
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name AAA Pharmaceutical, Inc.
Substance Name ACETAMINOPHEN
Strength Number 325
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Acetaminophen


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