NDC 11822-2350

Pain Relief Acetaminophen PM Extra Strength

Acetaminophen And Diphenhydramine Hcl

Pain Relief Acetaminophen PM Extra Strength is a Oral Tablet, Film Coated in the Human Otc Drug category. It is labeled and distributed by Rite Aid Corporation. The primary component is Acetaminophen; Diphenhydramine Hydrochloride.

Product ID11822-2350_35585315-6d2e-4420-a9ee-1dc4e6204b4c
NDC11822-2350
Product TypeHuman Otc Drug
Proprietary NamePain Relief Acetaminophen PM Extra Strength
Generic NameAcetaminophen And Diphenhydramine Hcl
Dosage FormTablet, Film Coated
Route of AdministrationORAL
Marketing Start Date1994-05-15
Marketing CategoryOTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
Application Numberpart343
Labeler NameRite Aid Corporation
Substance NameACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE
Active Ingredient Strength500 mg/1; mg/1
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 11822-2350-2

1 BOTTLE, PLASTIC in 1 CARTON (11822-2350-2) > 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
Marketing Start Date1994-05-15
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 11822-2350-7 [11822235007]

Pain Relief Acetaminophen PM Extra Strength TABLET, FILM COATED
Marketing CategoryOTC MONOGRAPH NOT FINAL
Application Numberpart343
Product TypeHUMAN OTC DRUG
Marketing Start Date1994-05-15

NDC 11822-2350-4 [11822235004]

Pain Relief Acetaminophen PM Extra Strength TABLET, FILM COATED
Marketing CategoryOTC MONOGRAPH NOT FINAL
Application Numberpart343
Product TypeHUMAN OTC DRUG
Marketing Start Date1994-05-15

NDC 11822-2350-1 [11822235001]

Pain Relief Acetaminophen PM Extra Strength TABLET, FILM COATED
Marketing CategoryOTC MONOGRAPH NOT FINAL
Application Numberpart343
Product TypeHUMAN OTC DRUG
Marketing Start Date1994-05-15
Marketing End Date2015-11-18

NDC 11822-2350-2 [11822235002]

Pain Relief Acetaminophen PM Extra Strength TABLET, FILM COATED
Marketing CategoryOTC MONOGRAPH NOT FINAL
Application Numberpart343
Product TypeHUMAN OTC DRUG
Marketing Start Date1994-05-15

NDC 11822-2350-5 [11822235005]

Pain Relief Acetaminophen PM Extra Strength TABLET, FILM COATED
Marketing CategoryOTC MONOGRAPH NOT FINAL
Application Numberpart343
Product TypeHUMAN OTC DRUG
Marketing Start Date1994-05-15

Drug Details

Active Ingredients

IngredientStrength
ACETAMINOPHEN500 mg/1

OpenFDA Data

SPL SET ID:17d27771-a112-474f-9a58-29af0d7e1af3
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 1092189
    • UPC Code
  • 0011822961332

    • NDC Crossover Matching brand name "Pain Relief Acetaminophen PM Extra Strength" or generic name "Acetaminophen And Diphenhydramine Hcl"

    NDCBrand NameGeneric Name
    0536-3479Acetaminophen and Diphenhydramine HClAcetaminophen and Diphenhydramine HCl
    49035-235Acetaminophen PMAcetaminophen and Diphenhydramine HCl
    55319-235Acetaminophen PMAcetaminophen and Diphenhydramine HCl
    55319-556Acetaminophen PMAcetaminophen and Diphenhydramine HCl
    58602-743Aurophen PM Extra StrengthAcetaminophen and Diphenhydramine HCl
    37205-759Extra Strength Pain Reliever PMAcetaminophen and Diphenhydramine HCl
    49738-999KMart - Pain Relief PMAcetaminophen and Diphenhydramine HCl
    11822-0556Pain Relief Acetaminophen PMAcetaminophen and Diphenhydramine HCl
    11822-2350Pain Relief Acetaminophen PMAcetaminophen and Diphenhydramine HCl
    21130-556Pain Relief PMAcetaminophen and Diphenhydramine HCl
    49738-655Pain Relief PMAcetaminophen and Diphenhydramine HCl
    55910-655Pain Relief PMAcetaminophen and Diphenhydramine HCl
    15127-325Pain Reliever PMAcetaminophen and Diphenhydramine HCl
    0135-0608PANADOLacetaminophen and diphenhydramine HCl
    0135-7021PANADOLacetaminophen and diphenhydramine HCl
    41250-556Rapid Release Pain Relief PMAcetaminophen and Diphenhydramine HCl
    0363-0235Wal-Nadol PMAcetaminophen and Diphenhydramine HCl
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