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 SOLUTION
Routes
ORAL
Active Ingredients

acetaminophen 1000 mg/30mL

Manufacturer
Major Pharmaceuticals

Identifiers & Regulatory

Product NDC 0904-7481
Product ID 0904-7481_62b95d8b-99ff-48bc-a816-d32a5e2d7706
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M013
Listing Expiration 2026-12-31
Marketing Start 2021-07-15

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 09047481
Hyphenated Format 0904-7481

Supplemental Identifiers

RxCUI
307684
UPC
0309047481590
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
  • 1000 mg/30mL
source: ndc
Packaging
  • 237 mL in 1 BOTTLE, PLASTIC (0904-7481-59)
source: ndc

Packages (1)

Ingredients (1)

acetaminophen (1000 mg/30mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "62b95d8b-99ff-48bc-a816-d32a5e2d7706", "openfda": {"upc": ["0309047481590"], "unii": ["362O9ITL9D"], "rxcui": ["307684"], "spl_set_id": ["e1a55e0d-bb86-4515-8436-51a74b403685"], "manufacturer_name": ["Major Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "237 mL in 1 BOTTLE, PLASTIC (0904-7481-59)", "package_ndc": "0904-7481-59", "marketing_start_date": "20210715"}], "brand_name": "Acetaminophen", "product_id": "0904-7481_62b95d8b-99ff-48bc-a816-d32a5e2d7706", "dosage_form": "SOLUTION", "product_ndc": "0904-7481", "generic_name": "Acetaminophen", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Acetaminophen", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "1000 mg/30mL"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20210715", "listing_expiration_date": "20261231"}