acetaminophen

Generic: acetaminophen

Labeler: mylan institutional llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name acetaminophen
Generic Name acetaminophen
Labeler mylan institutional llc
Dosage Form INJECTION, SOLUTION
Routes
INTRAVENOUS
Active Ingredients

acetaminophen 1000 mg/100mL

Manufacturer
Mylan Institutional LLC

Identifiers & Regulatory

Product NDC 67457-940
Product ID 67457-940_e19103ae-5be3-4e78-8a8c-93235f8e23ac
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA213255
Listing Expiration 2026-12-31
Marketing Start 2020-12-07

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 67457940
Hyphenated Format 67457-940

Supplemental Identifiers

RxCUI
483017
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 ANDA213255 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 1000 mg/100mL
source: ndc
Packaging
  • 24 BAG in 1 CARTON (67457-940-10) / 100 mL in 1 BAG
source: ndc

Packages (1)

Ingredients (1)

acetaminophen (1000 mg/100mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "e19103ae-5be3-4e78-8a8c-93235f8e23ac", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["483017"], "spl_set_id": ["1d456d07-fca2-4d43-92c0-f3b3c8b54420"], "manufacturer_name": ["Mylan Institutional LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "24 BAG in 1 CARTON (67457-940-10)  / 100 mL in 1 BAG", "package_ndc": "67457-940-10", "marketing_start_date": "20201207"}], "brand_name": "Acetaminophen", "product_id": "67457-940_e19103ae-5be3-4e78-8a8c-93235f8e23ac", "dosage_form": "INJECTION, SOLUTION", "product_ndc": "67457-940", "generic_name": "Acetaminophen", "labeler_name": "Mylan Institutional LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Acetaminophen", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "1000 mg/100mL"}], "application_number": "ANDA213255", "marketing_category": "ANDA", "marketing_start_date": "20201207", "listing_expiration_date": "20261231"}