acetaminophen
Generic: acetaminophen
Labeler: wal-mart stores incDrug Facts
Product Profile
Brand Name
acetaminophen
Generic Name
acetaminophen
Labeler
wal-mart stores inc
Dosage Form
TABLET
Routes
Active Ingredients
acetaminophen 650 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
79903-137
Product ID
79903-137_464fe001-f74a-8ac0-e063-6394a90ae5d7
Product Type
HUMAN OTC DRUG
Marketing Category
ANDA
Application Number
ANDA211544
Listing Expiration
2026-12-31
Marketing Start
2022-11-29
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
79903137
Hyphenated Format
79903-137
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
- 24 TABLET in 1 BOTTLE (79903-137-24)
- 100 TABLET in 1 BOTTLE (79903-137-99)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "464fe001-f74a-8ac0-e063-6394a90ae5d7", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["1148399"], "spl_set_id": ["e34d07b5-ccbb-cd14-e053-2a95a90a394b"], "manufacturer_name": ["WAL-MART STORES INC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "24 TABLET in 1 BOTTLE (79903-137-24)", "package_ndc": "79903-137-24", "marketing_start_date": "20221129"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (79903-137-99)", "package_ndc": "79903-137-99", "marketing_start_date": "20221129"}], "brand_name": "Acetaminophen", "product_id": "79903-137_464fe001-f74a-8ac0-e063-6394a90ae5d7", "dosage_form": "TABLET", "product_ndc": "79903-137", "generic_name": "Acetaminophen", "labeler_name": "WAL-MART STORES 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": "20221129", "listing_expiration_date": "20261231"}