extra strength acetaminophen

Generic: acetaminophen

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

Drug Facts

Product Profile

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

acetaminophen 500 mg/1

Manufacturer
NuCare Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 68071-3907
Product ID 68071-3907_4266d35a-cdb8-50f2-e063-6294a90a1002
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M013
Listing Expiration 2026-12-31
Marketing Start 2024-11-01

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 680713907
Hyphenated Format 68071-3907

Supplemental Identifiers

RxCUI
198440
UPC
0368071390759
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 extra strength acetaminophen (source: ndc)
Generic Name acetaminophen (source: ndc)
Application Number M013 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
source: ndc
Packaging
  • 20 TABLET in 1 BOTTLE (68071-3907-2)
  • 30 TABLET in 1 BOTTLE (68071-3907-3)
  • 45 TABLET in 1 BOTTLE (68071-3907-5)
source: ndc

Packages (3)

68071-3907-2 20 TABLET in 1 BOTTLE (68071-3907-2) 68071-3907-3 30 TABLET in 1 BOTTLE (68071-3907-3) 68071-3907-5 45 TABLET in 1 BOTTLE (68071-3907-5)

Ingredients (1)

acetaminophen (500 mg/1)

Linked Drug Pages (1)

Extra Strength Acetaminophen ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4266d35a-cdb8-50f2-e063-6294a90a1002", "openfda": {"upc": ["0368071390759"], "unii": ["362O9ITL9D"], "rxcui": ["198440"], "spl_set_id": ["41affa1a-5aac-7fc0-e063-6394a90a5557"], "manufacturer_name": ["NuCare Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET in 1 BOTTLE (68071-3907-2)", "package_ndc": "68071-3907-2", "marketing_start_date": "20251030"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (68071-3907-3)", "package_ndc": "68071-3907-3", "marketing_start_date": "20251030"}, {"sample": false, "description": "45 TABLET in 1 BOTTLE (68071-3907-5)", "package_ndc": "68071-3907-5", "marketing_start_date": "20251021"}], "brand_name": "Extra Strength Acetaminophen", "product_id": "68071-3907_4266d35a-cdb8-50f2-e063-6294a90a1002", "dosage_form": "TABLET", "product_ndc": "68071-3907", "generic_name": "Acetaminophen", "labeler_name": "NuCare Pharmaceuticals, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Extra Strength Acetaminophen", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/1"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20241101", "listing_expiration_date": "20261231"}