acetaminophen pm extra strength

Generic: acetaminophen, diphenhydramine hcl

Labeler: chain drug marketing association inc
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name acetaminophen pm extra strength
Generic Name acetaminophen, diphenhydramine hcl
Labeler chain drug marketing association inc
Dosage Form TABLET, COATED
Routes
ORAL
Active Ingredients

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

Manufacturer
CHAIN DRUG MARKETING ASSOCIATION INC

Identifiers & Regulatory

Product NDC 63868-210
Product ID 63868-210_c2a91066-4981-42c6-9a60-0841c1c3d2af
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M013
Marketing Start 2007-12-17
Marketing End 2026-12-31

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 63868210
Hyphenated Format 63868-210

Supplemental Identifiers

RxCUI
1092189
UPC
0635515993686
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 extra strength (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
  • 1 BOTTLE, PLASTIC in 1 CARTON (63868-210-20) / 20 TABLET, COATED in 1 BOTTLE, PLASTIC
source: ndc

Packages (1)

63868-210-20 1 BOTTLE, PLASTIC in 1 CARTON (63868-210-20) / 20 TABLET, COATED in 1 BOTTLE, PLASTIC

Ingredients (2)

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

Linked Drug Pages (1)

Acetaminophen PM Extra Strength ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "c2a91066-4981-42c6-9a60-0841c1c3d2af", "openfda": {"upc": ["0635515993686"], "unii": ["362O9ITL9D", "TC2D6JAD40"], "rxcui": ["1092189"], "spl_set_id": ["bbc704e5-79f6-4c72-846b-cc30c5c43cb4"], "manufacturer_name": ["CHAIN DRUG MARKETING ASSOCIATION INC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (63868-210-20)  / 20 TABLET, COATED in 1 BOTTLE, PLASTIC", "package_ndc": "63868-210-20", "marketing_end_date": "20261231", "marketing_start_date": "20071217"}], "brand_name": "Acetaminophen PM Extra Strength", "product_id": "63868-210_c2a91066-4981-42c6-9a60-0841c1c3d2af", "dosage_form": "TABLET, COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "63868-210", "generic_name": "Acetaminophen, Diphenhydramine HCl", "labeler_name": "CHAIN DRUG MARKETING ASSOCIATION INC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Acetaminophen PM", "brand_name_suffix": "Extra Strength", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/1"}, {"name": "DIPHENHYDRAMINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_end_date": "20261231", "marketing_start_date": "20071217"}