acetaminophen pm

Generic: acetaminophen 500mg / diphenhydramine hcl 25mg

Labeler: ulai health llc
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name acetaminophen pm
Generic Name acetaminophen 500mg / diphenhydramine hcl 25mg
Labeler ulai health llc
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

acetaminophen 500 mg/1, diphenhydramine hydrochloride 25 mg/1

Manufacturer
Ulai Health LLC

Identifiers & Regulatory

Product NDC 73057-352
Product ID 73057-352_2c27d537-a03c-3775-e063-6394a90ad003
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M013
Listing Expiration 2026-12-31
Marketing Start 2019-07-08

Pharmacologic Class

Classes
histamine h1 receptor antagonists [moa] histamine-1 receptor antagonist [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 73057352
Hyphenated Format 73057-352

Supplemental Identifiers

RxCUI
1092189
UPC
0373057352034
UNII
362O9ITL9D TC2D6JAD40

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name acetaminophen pm (source: ndc)
Generic Name acetaminophen 500mg / diphenhydramine hcl 25mg (source: ndc)
Application Number M013 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
  • 25 mg/1
source: ndc
Packaging
  • 24 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (73057-352-03)
source: ndc

Packages (1)

73057-352-03 24 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (73057-352-03)

Ingredients (2)

acetaminophen (500 mg/1) diphenhydramine hydrochloride (25 mg/1)

Linked Drug Pages (1)

ACETAMINOPHEN PM ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2c27d537-a03c-3775-e063-6394a90ad003", "openfda": {"upc": ["0373057352034"], "unii": ["362O9ITL9D", "TC2D6JAD40"], "rxcui": ["1092189"], "spl_set_id": ["d4a568c9-a721-48d1-aebc-fc65444947ce"], "manufacturer_name": ["Ulai Health LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "24 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (73057-352-03)", "package_ndc": "73057-352-03", "marketing_start_date": "20190708"}], "brand_name": "ACETAMINOPHEN PM", "product_id": "73057-352_2c27d537-a03c-3775-e063-6394a90ad003", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "73057-352", "generic_name": "Acetaminophen 500mg / Diphenhydramine HCl 25mg", "labeler_name": "Ulai Health LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "ACETAMINOPHEN PM", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/1"}, {"name": "DIPHENHYDRAMINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20190708", "listing_expiration_date": "20261231"}