tylenol pm extra strength

Generic: acetaminophen

Labeler: r j general corporation
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name tylenol pm extra strength
Generic Name acetaminophen
Labeler r j general corporation
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

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

Manufacturer
R J General Corporation

Identifiers & Regulatory

Product NDC 70264-028
Product ID 70264-028_43c8c37c-62db-f6e0-e063-6394a90aab46
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M013
Listing Expiration 2026-12-31
Marketing Start 2021-05-01

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 70264028
Hyphenated Format 70264-028

Supplemental Identifiers

RxCUI
1092189 1092378
UNII
362O9ITL9D TC2D6JAD40

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 tylenol pm extra strength (source: ndc)
Generic Name acetaminophen (source: ndc)
Application Number M013 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
  • 25 mg/1
source: ndc
Packaging
  • 50 POUCH in 1 BOX (70264-028-01) / 2 TABLET, FILM COATED in 1 POUCH
source: ndc

Packages (1)

70264-028-01 50 POUCH in 1 BOX (70264-028-01) / 2 TABLET, FILM COATED in 1 POUCH

Ingredients (2)

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

Linked Drug Pages (1)

TYLENOL PM EXTRA STRENGTH ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "43c8c37c-62db-f6e0-e063-6394a90aab46", "openfda": {"unii": ["362O9ITL9D", "TC2D6JAD40"], "rxcui": ["1092189", "1092378"], "spl_set_id": ["a40ea0e3-d666-4605-b5e0-beeaf8f586f2"], "manufacturer_name": ["R J General Corporation"]}, "finished": true, "packaging": [{"sample": false, "description": "50 POUCH in 1 BOX (70264-028-01)  / 2 TABLET, FILM COATED in 1 POUCH", "package_ndc": "70264-028-01", "marketing_start_date": "20210501"}], "brand_name": "TYLENOL PM EXTRA STRENGTH", "product_id": "70264-028_43c8c37c-62db-f6e0-e063-6394a90aab46", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "70264-028", "generic_name": "ACETAMINOPHEN", "labeler_name": "R J General Corporation", "product_type": "HUMAN OTC DRUG", "brand_name_base": "TYLENOL PM 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_start_date": "20210501", "listing_expiration_date": "20261231"}