tylenol extra strength
Generic: acetaminophen
Labeler: r j general corporationDrug Facts
Product Profile
Brand Name
tylenol extra strength
Generic Name
acetaminophen
Labeler
r j general corporation
Dosage Form
TABLET
Routes
Active Ingredients
acetaminophen 500 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
70264-027
Product ID
70264-027_43c8c03b-eb61-fccb-e063-6394a90a6211
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M013
Listing Expiration
2026-12-31
Marketing Start
2021-05-01
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
70264027
Hyphenated Format
70264-027
Supplemental Identifiers
RxCUI
UNII
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 extra strength (source: ndc)
Generic Name
acetaminophen (source: ndc)
Application Number
M013 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 500 mg/1
Packaging
- 50 POUCH in 1 BOX (70264-027-01) / 2 TABLET in 1 POUCH
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "43c8c03b-eb61-fccb-e063-6394a90a6211", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["198440", "209459"], "spl_set_id": ["99e45e83-37a3-44df-9a2a-98ba7457a5bb"], "manufacturer_name": ["R J General Corporation"]}, "finished": true, "packaging": [{"sample": false, "description": "50 POUCH in 1 BOX (70264-027-01) / 2 TABLET in 1 POUCH", "package_ndc": "70264-027-01", "marketing_start_date": "20210501"}], "brand_name": "TYLENOL EXTRA STRENGTH", "product_id": "70264-027_43c8c03b-eb61-fccb-e063-6394a90a6211", "dosage_form": "TABLET", "product_ndc": "70264-027", "generic_name": "ACETAMINOPHEN", "labeler_name": "R J General Corporation", "product_type": "HUMAN OTC DRUG", "brand_name_base": "TYLENOL EXTRA STRENGTH", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/1"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20210501", "listing_expiration_date": "20261231"}