acetaminophen
Generic: acetaminophen
Labeler: southern sales & service, inc.Drug Facts
Product Profile
Brand Name
acetaminophen
Generic Name
acetaminophen
Labeler
southern sales & service, inc.
Dosage Form
TABLET
Routes
Active Ingredients
acetaminophen 325 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
69822-692
Product ID
69822-692_0b57cdc0-3b62-26fd-e063-6394a90ad4fa
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M013
Listing Expiration
2026-12-31
Marketing Start
2019-01-01
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
69822692
Hyphenated Format
69822-692
Supplemental Identifiers
RxCUI
UPC
UNII
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
- 325 mg/1
Packaging
- 325 TABLET in 1 BOTTLE (69822-692-10)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "0b57cdc0-3b62-26fd-e063-6394a90ad4fa", "openfda": {"upc": ["0850011557235"], "unii": ["362O9ITL9D"], "rxcui": ["313782"], "spl_set_id": ["8b838af4-a74d-47b4-952e-dcf5598b08e1"], "manufacturer_name": ["Southern Sales & Service, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "325 TABLET in 1 BOTTLE (69822-692-10)", "package_ndc": "69822-692-10", "marketing_start_date": "20190101"}], "brand_name": "Acetaminophen", "product_id": "69822-692_0b57cdc0-3b62-26fd-e063-6394a90ad4fa", "dosage_form": "TABLET", "product_ndc": "69822-692", "generic_name": "ACETAMINOPHEN", "labeler_name": "Southern Sales & Service, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Acetaminophen", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "325 mg/1"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20190101", "listing_expiration_date": "20261231"}