acetaminophen
Generic: acetaminophen
Labeler: eugia us llcDrug Facts
Product Profile
Brand Name
acetaminophen
Generic Name
acetaminophen
Labeler
eugia us llc
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
acetaminophen 10 mg/mL
Manufacturer
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
UPC
UNII
Packaging Origin
Original Packager
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
source: ndc
Resolved Composition
Strengths
- 10 mg/mL
Packaging
- 24 VIAL, SINGLE-DOSE in 1 CARTON (55150-307-24) / 100 mL in 1 VIAL, SINGLE-DOSE (55150-307-01)
Packages (1)
Ingredients (1)
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"}