acetaminophen

Generic: acetaminophen

Labeler: hikma pharmaceuticals usa inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

acetaminophen 10 mg/mL

Manufacturer
Hikma Pharmaceuticals USA Inc.

Identifiers & Regulatory

Product NDC 24201-110
Product ID 24201-110_dfa24eae-037c-41c4-b423-96a3c1436fa4
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA202605
Listing Expiration 2027-12-31
Marketing Start 2023-03-01

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 24201110
Hyphenated Format 24201-110

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 ANDA202605 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 10 mg/mL
source: ndc
Packaging
  • 24 VIAL, GLASS in 1 CARTON (24201-110-24) / 100 mL in 1 VIAL, GLASS
source: ndc

Packages (1)

24201-110-24 24 VIAL, GLASS in 1 CARTON (24201-110-24) / 100 mL in 1 VIAL, GLASS

Ingredients (1)

acetaminophen (10 mg/mL)

Linked Drug Pages (1)

Acetaminophen ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "dfa24eae-037c-41c4-b423-96a3c1436fa4", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["483017"], "spl_set_id": ["7243bf2c-2c44-4dff-8a9e-d788d31dca86"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "24 VIAL, GLASS in 1 CARTON (24201-110-24)  / 100 mL in 1 VIAL, GLASS", "package_ndc": "24201-110-24", "marketing_start_date": "20230301"}], "brand_name": "Acetaminophen", "product_id": "24201-110_dfa24eae-037c-41c4-b423-96a3c1436fa4", "dosage_form": "INJECTION, SOLUTION", "product_ndc": "24201-110", "generic_name": "Acetaminophen", "labeler_name": "Hikma Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Acetaminophen", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "10 mg/mL"}], "application_number": "ANDA202605", "marketing_category": "ANDA", "marketing_start_date": "20230301", "listing_expiration_date": "20271231"}