acetaminophen
Generic: acetaminophen
Labeler: hf acquisition co llc, dba healthfirstDrug Facts
Product Profile
Brand Name
acetaminophen
Generic Name
acetaminophen
Labeler
hf acquisition co llc, dba healthfirst
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
acetaminophen 10 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
51662-1540
Product ID
51662-1540_1be60f10-f962-05a7-e063-6294a90aeb2c
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA210969
Listing Expiration
2026-12-31
Marketing Start
2022-04-09
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
516621540
Hyphenated Format
51662-1540
Supplemental Identifiers
RxCUI
UNII
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 POUCH in 1 CASE (51662-1540-3) / 1 VIAL, SINGLE-DOSE in 1 POUCH (51662-1540-2) / 100 mL in 1 VIAL, SINGLE-DOSE (51662-1540-1)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "1be60f10-f962-05a7-e063-6294a90aeb2c", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["483017"], "spl_set_id": ["dc42ab17-cd30-4d1a-e053-2995a90a86ea"], "manufacturer_name": ["HF Acquisition Co LLC, DBA HealthFirst"]}, "finished": true, "packaging": [{"sample": false, "description": "24 POUCH in 1 CASE (51662-1540-3) / 1 VIAL, SINGLE-DOSE in 1 POUCH (51662-1540-2) / 100 mL in 1 VIAL, SINGLE-DOSE (51662-1540-1)", "package_ndc": "51662-1540-3", "marketing_start_date": "20220409"}], "brand_name": "ACETAMINOPHEN", "product_id": "51662-1540_1be60f10-f962-05a7-e063-6294a90aeb2c", "dosage_form": "INJECTION, SOLUTION", "product_ndc": "51662-1540", "generic_name": "ACETAMINOPHEN", "labeler_name": "HF Acquisition Co LLC, DBA HealthFirst", "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": "20220409", "listing_expiration_date": "20261231"}