acetaminophen

Generic: acetaminophen

Labeler: cvs pharmacy
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name acetaminophen
Generic Name acetaminophen
Labeler cvs pharmacy
Dosage Form TABLET, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

acetaminophen 650 mg/1

Manufacturer
CVS Pharmacy

Identifiers & Regulatory

Product NDC 69842-930
Product ID 69842-930_2a40710a-b57f-9b21-e063-6294a90ad09d
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA078569
Listing Expiration 2026-12-31
Marketing Start 2012-12-21

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 69842930
Hyphenated Format 69842-930

Supplemental Identifiers

RxCUI
1148399
UPC
0050428257012
UNII
362O9ITL9D

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 (source: ndc)
Generic Name acetaminophen (source: ndc)
Application Number ANDA078569 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 650 mg/1
source: ndc
Packaging
  • 80 TABLET, EXTENDED RELEASE in 1 BOTTLE (69842-930-80)
source: ndc

Packages (1)

Ingredients (1)

acetaminophen (650 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2a40710a-b57f-9b21-e063-6294a90ad09d", "openfda": {"upc": ["0050428257012"], "unii": ["362O9ITL9D"], "rxcui": ["1148399"], "spl_set_id": ["6f880abe-5284-42b0-9db6-b071444b197b"], "manufacturer_name": ["CVS Pharmacy"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "80 TABLET, EXTENDED RELEASE in 1 BOTTLE (69842-930-80)", "package_ndc": "69842-930-80", "marketing_start_date": "20121221"}], "brand_name": "Acetaminophen", "product_id": "69842-930_2a40710a-b57f-9b21-e063-6294a90ad09d", "dosage_form": "TABLET, EXTENDED RELEASE", "product_ndc": "69842-930", "generic_name": "Acetaminophen", "labeler_name": "CVS Pharmacy", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Acetaminophen", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "650 mg/1"}], "application_number": "ANDA078569", "marketing_category": "ANDA", "marketing_start_date": "20121221", "listing_expiration_date": "20261231"}