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Acetaminophen PM - 57344-095-02 - (Acetaminophen and DIPHENHYDRAMINE HYDROCHLORIDE)

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Drug Information of Acetaminophen PM

Product NDC: 57344-095
Proprietary Name: Acetaminophen PM
Non Proprietary Name: Acetaminophen and DIPHENHYDRAMINE HYDROCHLORIDE
Active Ingredient(s): 500; 25    mg/1; mg/1 & nbsp;   Acetaminophen and DIPHENHYDRAMINE HYDROCHLORIDE
Administration Route(s): ORAL
Dosage Form(s): TABLET, COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Acetaminophen PM

Product NDC: 57344-095
Labeler Name: AAA Pharmaceutical, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part338
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20121213

Package Information of Acetaminophen PM

Package NDC: 57344-095-02
Package Description: 1 BOTTLE, PLASTIC in 1 CARTON (57344-095-02) > 50 TABLET, COATED in 1 BOTTLE, PLASTIC

NDC Information of Acetaminophen PM

NDC Code 57344-095-02
Proprietary Name Acetaminophen PM
Package Description 1 BOTTLE, PLASTIC in 1 CARTON (57344-095-02) > 50 TABLET, COATED in 1 BOTTLE, PLASTIC
Product NDC 57344-095
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen and DIPHENHYDRAMINE HYDROCHLORIDE
Dosage Form Name TABLET, COATED
Route Name ORAL
Start Marketing Date 20121213
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name AAA Pharmaceutical, Inc.
Substance Name ACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE
Strength Number 500; 25
Strength Unit mg/1; mg/1
Pharmaceutical Classes

Complete Information of Acetaminophen PM


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