acetaminophen

Generic: acetaminophen

Labeler: civica, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name acetaminophen
Generic Name acetaminophen
Labeler civica, inc.
Dosage Form INJECTION, SOLUTION
Routes
INTRAVENOUS
Active Ingredients

acetaminophen 10 mg/mL

Manufacturer
Civica, Inc.

Identifiers & Regulatory

Product NDC 72572-050
Product ID 72572-050_1b5ca3e0-ce08-4e11-9385-9ec22e5abb5b
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA204052
Listing Expiration 2026-12-31
Marketing Start 2022-11-10

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72572050
Hyphenated Format 72572-050

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 ANDA204052 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 10 mg/mL
source: ndc
Packaging
  • 10 VIAL, GLASS in 1 CARTON (72572-050-10) / 100 mL in 1 VIAL, GLASS (72572-050-01)
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": "1b5ca3e0-ce08-4e11-9385-9ec22e5abb5b", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["483017"], "spl_set_id": ["1b5ca3e0-ce08-4e11-9385-9ec22e5abb5b"], "manufacturer_name": ["Civica, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL, GLASS in 1 CARTON (72572-050-10)  / 100 mL in 1 VIAL, GLASS (72572-050-01)", "package_ndc": "72572-050-10", "marketing_start_date": "20221110"}], "brand_name": "Acetaminophen", "product_id": "72572-050_1b5ca3e0-ce08-4e11-9385-9ec22e5abb5b", "dosage_form": "INJECTION, SOLUTION", "product_ndc": "72572-050", "generic_name": "acetaminophen", "labeler_name": "Civica, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Acetaminophen", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "10 mg/mL"}], "application_number": "ANDA204052", "marketing_category": "ANDA", "marketing_start_date": "20221110", "listing_expiration_date": "20261231"}