NDC 58602-743

Aurophen PM Extra Strength

Acetaminophen And Diphenhydramine Hcl

Aurophen PM Extra Strength is a Oral Tablet in the Human Otc Drug category. It is labeled and distributed by Aurohealth Llc. The primary component is Acetaminophen; Diphenhydramine Hydrochloride.

Product ID58602-743_8595be52-a66c-412b-b771-e6cad3623d69
NDC58602-743
Product TypeHuman Otc Drug
Proprietary NameAurophen PM Extra Strength
Generic NameAcetaminophen And Diphenhydramine Hcl
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2016-02-24
Marketing CategoryOTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
Application Numberpart343
Labeler NameAurohealth LLC
Substance NameACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE
Active Ingredient Strength500 mg/1; mg/1
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 58602-743-07

1 BOTTLE in 1 CARTON (58602-743-07) > 24 TABLET in 1 BOTTLE
Marketing Start Date2016-02-24
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 58602-743-07 [58602074307]

Aurophen PM Extra Strength TABLET
Marketing CategoryOTC MONOGRAPH NOT FINAL
Application Numberpart343
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-02-24

NDC 58602-743-21 [58602074321]

Aurophen PM Extra Strength TABLET
Marketing CategoryOTC MONOGRAPH NOT FINAL
Application Numberpart343
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-02-24

NDC 58602-743-34 [58602074334]

Aurophen PM Extra Strength TABLET
Marketing CategoryOTC MONOGRAPH NOT FINAL
Application Numberpart343
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-02-24

NDC 58602-743-29 [58602074329]

Aurophen PM Extra Strength TABLET
Marketing CategoryOTC MONOGRAPH NOT FINAL
Application Numberpart343
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-02-24

NDC 58602-743-35 [58602074335]

Aurophen PM Extra Strength TABLET
Marketing CategoryOTC MONOGRAPH NOT FINAL
Application Numberpart343
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-02-24

NDC 58602-743-14 [58602074314]

Aurophen PM Extra Strength TABLET
Marketing CategoryOTC MONOGRAPH NOT FINAL
Application Numberpart343
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-02-24

Drug Details

Active Ingredients

IngredientStrength
ACETAMINOPHEN500 mg/1

OpenFDA Data

SPL SET ID:994351af-0c08-436f-a623-149ff7c7c463
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 1092189

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

    NDCBrand NameGeneric Name
    58602-743Aurophen PM Extra StrengthAcetaminophen and Diphenhydramine HCl
    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
    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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