acetaminophen
Generic: acetaminophen
Labeler: cvs pharmacy, inc.Drug Facts
Product Profile
Brand Name
acetaminophen
Generic Name
acetaminophen
Labeler
cvs pharmacy, inc.
Dosage Form
TABLET
Routes
Active Ingredients
acetaminophen 500 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
69842-465
Product ID
69842-465_373dfe36-0549-5035-e063-6394a90ac1df
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M013
Listing Expiration
2026-12-31
Marketing Start
2018-08-06
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
69842465
Hyphenated Format
69842-465
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
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 (source: ndc)
Generic Name
acetaminophen (source: ndc)
Application Number
M013 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 500 mg/1
Packaging
- 1 BOTTLE in 1 CARTON (69842-465-12) / 100 TABLET in 1 BOTTLE
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "373dfe36-0549-5035-e063-6394a90ac1df", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["198440"], "spl_set_id": ["6dea9e11-ff99-63c7-e053-2a91aa0a5b54"], "manufacturer_name": ["CVS Pharmacy, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (69842-465-12) / 100 TABLET in 1 BOTTLE", "package_ndc": "69842-465-12", "marketing_start_date": "20180806"}], "brand_name": "Acetaminophen", "product_id": "69842-465_373dfe36-0549-5035-e063-6394a90ac1df", "dosage_form": "TABLET", "product_ndc": "69842-465", "generic_name": "Acetaminophen", "labeler_name": "CVS Pharmacy, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Acetaminophen", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/1"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20180806", "listing_expiration_date": "20261231"}