acetaminophen

Generic: acetaminophen

Labeler: eugia us llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name acetaminophen
Generic Name acetaminophen
Labeler eugia us llc
Dosage Form INJECTION, SOLUTION
Routes
INTRAVENOUS
Active Ingredients

acetaminophen 10 mg/mL

Manufacturer
Eugia US LLC

Identifiers & Regulatory

Product NDC 55150-307
Product ID 55150-307_ddbd820d-6245-44a7-b539-3c6813ffa58a
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA210969
Listing Expiration 2026-12-31
Marketing Start 2020-10-21

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 55150307
Hyphenated Format 55150-307

Supplemental Identifiers

RxCUI
483017
UPC
0355150307012
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 ANDA210969 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 10 mg/mL
source: ndc
Packaging
  • 24 VIAL, SINGLE-DOSE in 1 CARTON (55150-307-24) / 100 mL in 1 VIAL, SINGLE-DOSE (55150-307-01)
source: ndc

Packages (1)

Ingredients (1)

acetaminophen (10 mg/mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "ddbd820d-6245-44a7-b539-3c6813ffa58a", "openfda": {"upc": ["0355150307012"], "unii": ["362O9ITL9D"], "rxcui": ["483017"], "spl_set_id": ["f80b6f72-f280-4b4a-a6a9-e6490b94705b"], "manufacturer_name": ["Eugia US LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "24 VIAL, SINGLE-DOSE in 1 CARTON (55150-307-24)  / 100 mL in 1 VIAL, SINGLE-DOSE (55150-307-01)", "package_ndc": "55150-307-24", "marketing_start_date": "20201021"}], "brand_name": "Acetaminophen", "product_id": "55150-307_ddbd820d-6245-44a7-b539-3c6813ffa58a", "dosage_form": "INJECTION, SOLUTION", "product_ndc": "55150-307", "generic_name": "Acetaminophen", "labeler_name": "Eugia US LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Acetaminophen", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "10 mg/mL"}], "application_number": "ANDA210969", "marketing_category": "ANDA", "marketing_start_date": "20201021", "listing_expiration_date": "20261231"}