acetaminophen diphenhydramine hcl

Generic: acetaminophen diphenhydramine hcl

Labeler: walgreens co.
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name acetaminophen diphenhydramine hcl
Generic Name acetaminophen diphenhydramine hcl
Labeler walgreens co.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

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

Manufacturer
WALGREENS CO.

Identifiers & Regulatory

Product NDC 0363-9664
Product ID 0363-9664_46537594-decc-ce80-e063-6394a90aa159
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M013
Listing Expiration 2026-12-31
Marketing Start 2022-09-30

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 03639664
Hyphenated Format 0363-9664

Supplemental Identifiers

RxCUI
1092189
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 diphenhydramine hcl (source: ndc)
Generic Name acetaminophen diphenhydramine hcl (source: ndc)
Application Number M013 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
  • 25 mg/1
source: ndc
Packaging
  • 375 TABLET in 1 BOTTLE (0363-9664-37)
  • 125 TABLET in 1 BOTTLE (0363-9664-60)
source: ndc

Packages (2)

0363-9664-37 375 TABLET in 1 BOTTLE (0363-9664-37) 0363-9664-60 125 TABLET in 1 BOTTLE (0363-9664-60)

Ingredients (2)

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

Linked Drug Pages (1)

Acetaminophen Diphenhydramine HCL ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "46537594-decc-ce80-e063-6394a90aa159", "openfda": {"unii": ["362O9ITL9D", "TC2D6JAD40"], "rxcui": ["1092189"], "spl_set_id": ["d92d97a8-0ee3-1206-e053-2a95a90a72a8"], "manufacturer_name": ["WALGREENS CO."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "375 TABLET in 1 BOTTLE (0363-9664-37)", "package_ndc": "0363-9664-37", "marketing_start_date": "20240713"}, {"sample": false, "description": "125 TABLET in 1 BOTTLE (0363-9664-60)", "package_ndc": "0363-9664-60", "marketing_start_date": "20220930"}], "brand_name": "Acetaminophen Diphenhydramine HCL", "product_id": "0363-9664_46537594-decc-ce80-e063-6394a90aa159", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "0363-9664", "generic_name": "Acetaminophen Diphenhydramine HCL", "labeler_name": "WALGREENS CO.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Acetaminophen Diphenhydramine HCL", "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": "20220930", "listing_expiration_date": "20261231"}