acetaminophen

Generic: acetaminophen

Labeler: major pharmaceuticals
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name acetaminophen
Generic Name acetaminophen
Labeler major pharmaceuticals
Dosage Form TABLET
Routes
ORAL
Active Ingredients

acetaminophen 325 mg/1

Manufacturer
Major Pharmaceuticals

Identifiers & Regulatory

Product NDC 0904-6773
Product ID 0904-6773_1134bfa6-67e9-ae56-e063-6294a90a16f3
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M013
Listing Expiration 2026-12-31
Marketing Start 2018-10-23

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 09046773
Hyphenated Format 0904-6773

Supplemental Identifiers

RxCUI
313782
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 M013 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 325 mg/1
source: ndc
Packaging
  • 10 BLISTER PACK in 1 BOX, UNIT-DOSE (0904-6773-61) / 10 TABLET in 1 BLISTER PACK
source: ndc

Packages (1)

Ingredients (1)

acetaminophen (325 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "1134bfa6-67e9-ae56-e063-6294a90a16f3", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["313782"], "spl_set_id": ["780aad35-d0f1-44b1-e053-2991aa0af9a7"], "manufacturer_name": ["Major Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 BLISTER PACK in 1 BOX, UNIT-DOSE (0904-6773-61)  / 10 TABLET in 1 BLISTER PACK", "package_ndc": "0904-6773-61", "marketing_start_date": "20181023"}], "brand_name": "Acetaminophen", "product_id": "0904-6773_1134bfa6-67e9-ae56-e063-6294a90a16f3", "dosage_form": "TABLET", "product_ndc": "0904-6773", "generic_name": "Acetaminophen", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Acetaminophen", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "325 mg/1"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20181023", "listing_expiration_date": "20261231"}