acetaminophen extra strength

Generic: acetaminophen

Labeler: bi-mart
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name acetaminophen extra strength
Generic Name acetaminophen
Labeler bi-mart
Dosage Form TABLET
Routes
ORAL
Active Ingredients

acetaminophen 500 mg/1

Manufacturer
Bi-Mart

Identifiers & Regulatory

Product NDC 37835-507
Product ID 37835-507_371d5ff5-bfe9-1a6f-e063-6294a90a3b19
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M013
Listing Expiration 2026-12-31
Marketing Start 2025-05-01

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 37835507
Hyphenated Format 37835-507

Supplemental Identifiers

RxCUI
198440
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 extra strength (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
  • 100 TABLET in 1 BOTTLE (37835-507-01)
  • 500 TABLET in 1 BOTTLE (37835-507-05)
  • 250 TABLET in 1 BOTTLE (37835-507-25)
source: ndc

Packages (3)

37835-507-01 100 TABLET in 1 BOTTLE (37835-507-01) 37835-507-05 500 TABLET in 1 BOTTLE (37835-507-05) 37835-507-25 250 TABLET in 1 BOTTLE (37835-507-25)

Ingredients (1)

acetaminophen (500 mg/1)

Linked Drug Pages (1)

Acetaminophen Extra Strength ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "371d5ff5-bfe9-1a6f-e063-6294a90a3b19", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["198440"], "spl_set_id": ["35483db0-d6b8-4b37-8113-1dbe51e42ae5"], "manufacturer_name": ["Bi-Mart"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (37835-507-01)", "package_ndc": "37835-507-01", "marketing_start_date": "20250501"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (37835-507-05)", "package_ndc": "37835-507-05", "marketing_start_date": "20250501"}, {"sample": false, "description": "250 TABLET in 1 BOTTLE (37835-507-25)", "package_ndc": "37835-507-25", "marketing_start_date": "20250501"}], "brand_name": "Acetaminophen Extra Strength", "product_id": "37835-507_371d5ff5-bfe9-1a6f-e063-6294a90a3b19", "dosage_form": "TABLET", "product_ndc": "37835-507", "generic_name": "Acetaminophen", "labeler_name": "Bi-Mart", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Acetaminophen Extra Strength", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/1"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20250501", "listing_expiration_date": "20261231"}