acetaminophen
Generic: acetaminophen
Labeler: cvs pharmacy, inc.Drug Facts
Product Profile
Brand Name
acetaminophen
Generic Name
acetaminophen
Labeler
cvs pharmacy, inc.
Dosage Form
TABLET, EXTENDED RELEASE
Routes
Active Ingredients
acetaminophen 650 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
69842-037
Product ID
69842-037_3ac76330-16d2-44f6-b013-8683059b83a9
Product Type
HUMAN OTC DRUG
Marketing Category
ANDA
Application Number
ANDA207229
Listing Expiration
2026-12-31
Marketing Start
2020-12-23
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
69842037
Hyphenated Format
69842-037
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
ANDA207229 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 650 mg/1
Packaging
- 225 TABLET, EXTENDED RELEASE in 1 BOTTLE (69842-037-35)
- 400 TABLET, EXTENDED RELEASE in 1 BOTTLE (69842-037-44)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3ac76330-16d2-44f6-b013-8683059b83a9", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["1148399"], "spl_set_id": ["b70beee4-407e-547c-e053-2a95a90af22a"], "manufacturer_name": ["CVS Pharmacy, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "225 TABLET, EXTENDED RELEASE in 1 BOTTLE (69842-037-35)", "package_ndc": "69842-037-35", "marketing_start_date": "20201223"}, {"sample": false, "description": "400 TABLET, EXTENDED RELEASE in 1 BOTTLE (69842-037-44)", "package_ndc": "69842-037-44", "marketing_start_date": "20201223"}], "brand_name": "Acetaminophen", "product_id": "69842-037_3ac76330-16d2-44f6-b013-8683059b83a9", "dosage_form": "TABLET, EXTENDED RELEASE", "product_ndc": "69842-037", "generic_name": "Acetaminophen", "labeler_name": "CVS Pharmacy, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Acetaminophen", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "650 mg/1"}], "application_number": "ANDA207229", "marketing_category": "ANDA", "marketing_start_date": "20201223", "listing_expiration_date": "20261231"}