apap

Generic: acetaminophen

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

Drug Facts

Product Profile

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

acetaminophen 500 mg/1

Manufacturer
Advance Pharmaceutical Inc.

Identifiers & Regulatory

Product NDC 17714-013
Product ID 17714-013_60f41580-e099-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 17714013
Hyphenated Format 17714-013

Supplemental Identifiers

RxCUI
198440
UPC
0017714013011 0017714013103
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 apap (source: ndc)
Generic Name acetaminophen (source: ndc)
Application Number part343 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (17714-013-01)
  • 1000 TABLET in 1 BOTTLE (17714-013-10)
source: ndc

Packages (2)

17714-013-01 100 TABLET in 1 BOTTLE (17714-013-01) 17714-013-10 1000 TABLET in 1 BOTTLE (17714-013-10)

Ingredients (1)

acetaminophen (500 mg/1)

Linked Drug Pages (1)

APAP ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "60f41580-e099-faad-e053-2a91aa0a9076", "openfda": {"upc": ["0017714013011", "0017714013103"], "unii": ["362O9ITL9D"], "rxcui": ["198440"], "spl_set_id": ["aba26f0a-94e4-4919-a3b0-033e3a9598ef"], "manufacturer_name": ["Advance Pharmaceutical Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (17714-013-01)", "package_ndc": "17714-013-01", "marketing_start_date": "19890205"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (17714-013-10)", "package_ndc": "17714-013-10", "marketing_start_date": "19890205"}], "brand_name": "APAP", "product_id": "17714-013_60f41580-e099-faad-e053-2a91aa0a9076", "dosage_form": "TABLET", "product_ndc": "17714-013", "generic_name": "Acetaminophen", "labeler_name": "Advance Pharmaceutical Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "APAP", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/1"}], "application_number": "part343", "marketing_category": "OTC MONOGRAPH NOT FINAL", "marketing_start_date": "19890205", "listing_expiration_date": "20261231"}