acetaminophen

Generic: acetaminophen

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

Drug Facts

Product Profile

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

acetaminophen 10 mg/mL

Manufacturer
REMEDYREPACK INC.

Identifiers & Regulatory

Product NDC 70518-4184
Product ID 70518-4184_3ff14a1e-fe75-90c9-e063-6294a90a7e24
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA210969
Listing Expiration 2026-12-31
Marketing Start 2024-09-24

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 705184184
Hyphenated Format 70518-4184

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
  • 25 VIAL, SINGLE-DOSE in 1 CARTON (70518-4184-2) / 100 mL in 1 VIAL, SINGLE-DOSE (70518-4184-3)
source: ndc

Packages (1)

70518-4184-2 25 VIAL, SINGLE-DOSE in 1 CARTON (70518-4184-2) / 100 mL in 1 VIAL, SINGLE-DOSE (70518-4184-3)

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": "3ff14a1e-fe75-90c9-e063-6294a90a7e24", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["483017"], "spl_set_id": ["464e404a-1957-44a2-a53a-f2a9d3c15bde"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL, SINGLE-DOSE in 1 CARTON (70518-4184-2)  / 100 mL in 1 VIAL, SINGLE-DOSE (70518-4184-3)", "package_ndc": "70518-4184-2", "marketing_start_date": "20240930"}], "brand_name": "Acetaminophen", "product_id": "70518-4184_3ff14a1e-fe75-90c9-e063-6294a90a7e24", "dosage_form": "INJECTION, SOLUTION", "product_ndc": "70518-4184", "generic_name": "Acetaminophen", "labeler_name": "REMEDYREPACK INC.", "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": "20240924", "listing_expiration_date": "20261231"}