acetaminophen

Generic: acetaminophen

Labeler: hf acquisition co llc, dba healthfirst
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name acetaminophen
Generic Name acetaminophen
Labeler hf acquisition co llc, dba healthfirst
Dosage Form INJECTION, SOLUTION
Routes
INTRAVENOUS
Active Ingredients

acetaminophen 10 mg/mL

Manufacturer
HF Acquisition Co LLC, DBA HealthFirst

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
483017
UNII
362O9ITL9D

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 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)
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": "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"}