NDC 57344-095

Acetaminophen PM

Acetaminophen And Diphenhydramine Hydrochloride

Acetaminophen PM is a Oral Tablet, Coated in the Human Otc Drug category. It is labeled and distributed by Aaa Pharmaceutical, Inc.. The primary component is Acetaminophen; Diphenhydramine Hydrochloride.

Product ID57344-095_052c52a3-1bc5-499c-8cc8-b28c1547bd7d
NDC57344-095
Product TypeHuman Otc Drug
Proprietary NameAcetaminophen PM
Generic NameAcetaminophen And Diphenhydramine Hydrochloride
Dosage FormTablet, Coated
Route of AdministrationORAL
Marketing Start Date2012-12-13
Marketing CategoryOTC MONOGRAPH FINAL / OTC MONOGRAPH FINAL
Application Numberpart338
Labeler NameAAA Pharmaceutical, Inc.
Substance NameACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE
Active Ingredient Strength500 mg/1; mg/1
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 57344-095-01

1 BOTTLE, PLASTIC in 1 CARTON (57344-095-01) > 24 TABLET, COATED in 1 BOTTLE, PLASTIC
Marketing Start Date2017-07-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 57344-095-02 [57344009502]

Acetaminophen PM TABLET, COATED
Marketing CategoryOTC monograph final
Application Numberpart341
Product TypeHUMAN OTC DRUG
Marketing Start Date2012-10-01

NDC 57344-095-09 [57344009509]

Acetaminophen PM TABLET, COATED
Marketing CategoryOTC monograph final
Application Numberpart341
Product TypeHUMAN OTC DRUG
Marketing Start Date2012-10-01
Marketing End Date2019-09-11

NDC 57344-095-01 [57344009501]

Acetaminophen PM TABLET, COATED
Marketing CategoryOTC monograph final
Application Numberpart341
Product TypeHUMAN OTC DRUG
Marketing Start Date2017-07-01

NDC 57344-095-08 [57344009508]

Acetaminophen PM TABLET, COATED
Marketing CategoryOTC monograph final
Application Numberpart341
Product TypeHUMAN OTC DRUG
Marketing Start Date2012-10-01
Marketing End Date2019-09-11

NDC 57344-095-06 [57344009506]

Acetaminophen PM TABLET, COATED
Marketing CategoryOTC monograph final
Application Numberpart341
Product TypeHUMAN OTC DRUG
Marketing Start Date2012-10-01
Marketing End Date2019-09-11

NDC 57344-095-04 [57344009504]

Acetaminophen PM TABLET, COATED
Marketing CategoryOTC monograph final
Application Numberpart341
Product TypeHUMAN OTC DRUG
Marketing Start Date2012-10-01
Marketing End Date2019-09-11

NDC 57344-095-12 [57344009512]

Acetaminophen PM TABLET, COATED
Marketing CategoryOTC monograph final
Application Numberpart341
Product TypeHUMAN OTC DRUG
Marketing Start Date2012-10-01
Marketing End Date2019-09-11

NDC 57344-095-07 [57344009507]

Acetaminophen PM TABLET, COATED
Marketing CategoryOTC monograph final
Application Numberpart341
Product TypeHUMAN OTC DRUG
Marketing Start Date2012-10-01
Marketing End Date2019-09-11

NDC 57344-095-03 [57344009503]

Acetaminophen PM TABLET, COATED
Marketing CategoryOTC monograph final
Application Numberpart341
Product TypeHUMAN OTC DRUG
Marketing Start Date2017-11-01

Drug Details

Active Ingredients

IngredientStrength
ACETAMINOPHEN500 mg/1

OpenFDA Data

SPL SET ID:409b5fcd-5880-4dda-85d8-26aeceb4f8ab
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 1092189

    • NDC Crossover Matching brand name "Acetaminophen PM" or generic name "Acetaminophen And Diphenhydramine Hydrochloride"

    NDCBrand NameGeneric Name
    11673-556Acetaminophen PMAcetaminophen, Diphenhydramine HCl
    11822-0556Acetaminophen PMAcetaminophen and Diphenhydramine HCl
    17714-133ACETAMINOPHEN PMACETAMINOPHEN PM
    21130-360Acetaminophen PMAcetaminophen, Diphenhydramine HCl
    30142-530acetaminophen pmAcetaminophen, Diphenhydramine HCl
    30142-700acetaminophen pmAcetaminophen, Diphenhydramine HCl
    30142-800acetaminophen pmAcetaminophen, Diphenhydramine HCl
    37012-771Acetaminophen PMAcetaminophen and Diphenhydramine Hydrochloride
    41163-228Acetaminophen PMAcetaminophen, Diphenhydramine HCl
    41163-515Acetaminophen PMAcetaminophen and Diphenhydramine Hydrochloride
    41163-956Acetaminophen PMAcetaminophen, Diphenhydramine HCl
    69842-758Acetaminophen PMAcetaminophen PM
    42912-0154Acetaminophen PMAcetaminophen PM
    57344-095Acetaminophen PMAcetaminophen PM
    67510-0154Acetaminophen PMAcetaminophen PM
    73057-352ACETAMINOPHEN PMACETAMINOPHEN PM
    72036-171Acetaminophen PMAcetaminophen PM
    0536-1003ACETA-GESICACETAMINOPHEN AND DIPHENHYDRAMINE HYDROCHLORIDE
    30142-193Acetaminophen and Diphenhydramine hydrochlorideAcetaminophen and Diphenhydramine hydrochloride
    30142-755Extra Strength Acetaminophen PMAcetaminophen and Diphenhydramine Hydrochloride
    21130-095Pain Relief PMAcetaminophen and Diphenhydramine Hydrochloride
    36800-095Pain Relief PMAcetaminophen and Diphenhydramine Hydrochloride
    36800-771Pain Relief PMAcetaminophen and Diphenhydramine Hydrochloride
    37808-795Pain Relief PMAcetaminophen and Diphenhydramine Hydrochloride
    41250-195pain relief PMAcetaminophen and Diphenhydramine Hydrochloride
    15127-033Pain Reliever PMAcetaminophen and Diphenhydramine Hydrochloride
    0031-8770Robitussin Honey Severe Cough, Flu Plus Sore Throat Nighttimeacetaminophen and diphenhydramine hydrochloride
    41167-0040Unisom PM Pain Nighttime Sleep Aid and Pain RelieverAcetaminophen and Diphenhydramine Hydrochloride
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