acetaminophen

Generic: acetaminophen

Labeler: advance pharmaceutical inc.
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH NOT FINAL Inactive Finished

Drug Facts

Product Profile

Brand Name acetaminophen
Generic Name acetaminophen
Labeler advance pharmaceutical inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

acetaminophen 325 mg/1

Manufacturer
Advance Pharmaceutical Inc.

Identifiers & Regulatory

Product NDC 17714-012
Product ID 17714-012_60f41580-e068-faad-e053-2a91aa0a9076
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH NOT FINAL
Application Number part343
Listing Expiration 2026-12-31
Marketing Start 1989-02-05

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 17714012
Hyphenated Format 17714-012

Supplemental Identifiers

RxCUI
313782
UPC
0017714012014
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 part343 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 325 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (17714-012-01)
  • 1000 TABLET in 1 BOTTLE (17714-012-10)
source: ndc

Packages (2)

17714-012-01 100 TABLET in 1 BOTTLE (17714-012-01) 17714-012-10 1000 TABLET in 1 BOTTLE (17714-012-10)

Ingredients (1)

acetaminophen (325 mg/1)

Linked Drug Pages (1)

Acetaminophen ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "60f41580-e068-faad-e053-2a91aa0a9076", "openfda": {"upc": ["0017714012014"], "unii": ["362O9ITL9D"], "rxcui": ["313782"], "spl_set_id": ["3793a17e-13bf-4d27-b8fa-6753b760f820"], "manufacturer_name": ["Advance Pharmaceutical Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (17714-012-01)", "package_ndc": "17714-012-01", "marketing_start_date": "19890205"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (17714-012-10)", "package_ndc": "17714-012-10", "marketing_start_date": "19890205"}], "brand_name": "Acetaminophen", "product_id": "17714-012_60f41580-e068-faad-e053-2a91aa0a9076", "dosage_form": "TABLET", "product_ndc": "17714-012", "generic_name": "Acetaminophen", "labeler_name": "Advance Pharmaceutical Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Acetaminophen", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "325 mg/1"}], "application_number": "part343", "marketing_category": "OTC MONOGRAPH NOT FINAL", "marketing_start_date": "19890205", "listing_expiration_date": "20261231"}