acetaminophen

Generic: extra strength pain relief

Labeler: nucare pharmaceuticals,inc.
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name acetaminophen
Generic Name extra strength pain relief
Labeler nucare pharmaceuticals,inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

acetaminophen 500 mg/1

Manufacturer
NuCare Pharmaceuticals,Inc.

Identifiers & Regulatory

Product NDC 68071-5239
Product ID 68071-5239_2a95afd1-cd26-371c-e063-6294a90a97d4
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M007
Listing Expiration 2026-12-31
Marketing Start 1989-01-01

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 680715239
Hyphenated Format 68071-5239

Supplemental Identifiers

RxCUI
198440
UPC
0368071523935
UNII
362O9ITL9D

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 extra strength pain relief (source: ndc)
Application Number M007 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (68071-5239-3)
  • 45 TABLET in 1 BOTTLE (68071-5239-5)
  • 90 TABLET in 1 BOTTLE (68071-5239-9)
source: ndc

Packages (3)

68071-5239-3 30 TABLET in 1 BOTTLE (68071-5239-3) 68071-5239-5 45 TABLET in 1 BOTTLE (68071-5239-5) 68071-5239-9 90 TABLET in 1 BOTTLE (68071-5239-9)

Ingredients (1)

acetaminophen (500 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": "2a95afd1-cd26-371c-e063-6294a90a97d4", "openfda": {"upc": ["0368071523935"], "unii": ["362O9ITL9D"], "rxcui": ["198440"], "spl_set_id": ["a32f346e-71d0-cc11-e053-2a95a90ae88c"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (68071-5239-3)", "package_ndc": "68071-5239-3", "marketing_start_date": "20200413"}, {"sample": false, "description": "45 TABLET in 1 BOTTLE (68071-5239-5)", "package_ndc": "68071-5239-5", "marketing_start_date": "20200413"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (68071-5239-9)", "package_ndc": "68071-5239-9", "marketing_start_date": "20200413"}], "brand_name": "Acetaminophen", "product_id": "68071-5239_2a95afd1-cd26-371c-e063-6294a90a97d4", "dosage_form": "TABLET", "product_ndc": "68071-5239", "generic_name": "Extra Strength Pain Relief", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Acetaminophen", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/1"}], "application_number": "M007", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "19890101", "listing_expiration_date": "20261231"}