acetaminophen
Generic: acetaminophen
Labeler: leader/ cardinal health 110, incDrug Facts
Product Profile
Brand Name
acetaminophen
Generic Name
acetaminophen
Labeler
leader/ cardinal health 110, inc
Dosage Form
TABLET
Routes
Active Ingredients
acetaminophen 650 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
70000-0626
Product ID
70000-0626_46532c1b-4ecc-d854-e063-6294a90a35ac
Product Type
HUMAN OTC DRUG
Marketing Category
ANDA
Application Number
ANDA211544
Listing Expiration
2026-12-31
Marketing Start
2023-03-02
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
700000626
Hyphenated Format
70000-0626
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
ANDA211544 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 650 mg/1
Packaging
- 100 TABLET in 1 BOTTLE (70000-0626-1)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "46532c1b-4ecc-d854-e063-6294a90a35ac", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["1148399"], "spl_set_id": ["f5dc335d-d3cf-ba94-e053-2a95a90ac6d3"], "manufacturer_name": ["LEADER/ Cardinal Health 110, Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (70000-0626-1)", "package_ndc": "70000-0626-1", "marketing_start_date": "20230302"}], "brand_name": "Acetaminophen", "product_id": "70000-0626_46532c1b-4ecc-d854-e063-6294a90a35ac", "dosage_form": "TABLET", "product_ndc": "70000-0626", "generic_name": "Acetaminophen", "labeler_name": "LEADER/ Cardinal Health 110, Inc", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Acetaminophen", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "650 mg/1"}], "application_number": "ANDA211544", "marketing_category": "ANDA", "marketing_start_date": "20230302", "listing_expiration_date": "20261231"}