acetaminophen

Generic: acetaminophen

Labeler: sandoz inc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

acetaminophen 10 mg/mL

Manufacturer
Sandoz Inc

Identifiers & Regulatory

Product NDC 0781-3156
Product ID 0781-3156_a309db84-6691-4628-85f9-750bba002be9
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA204052
Listing Expiration 2026-12-31
Marketing Start 2020-12-06

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 07813156
Hyphenated Format 0781-3156

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 (0781-3156-95) / 100 mL in 1 VIAL, GLASS (0781-3156-06)
source: ndc

Packages (1)

0781-3156-95 10 VIAL, GLASS in 1 CARTON (0781-3156-95) / 100 mL in 1 VIAL, GLASS (0781-3156-06)

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": "a309db84-6691-4628-85f9-750bba002be9", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["483017"], "spl_set_id": ["3b4ab1cf-8642-44f5-b3a2-3f1f7c620ce9"], "manufacturer_name": ["Sandoz Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL, GLASS in 1 CARTON (0781-3156-95)  / 100 mL in 1 VIAL, GLASS (0781-3156-06)", "package_ndc": "0781-3156-95", "marketing_start_date": "20201206"}], "brand_name": "Acetaminophen", "product_id": "0781-3156_a309db84-6691-4628-85f9-750bba002be9", "dosage_form": "INJECTION, SOLUTION", "product_ndc": "0781-3156", "generic_name": "acetaminophen", "labeler_name": "Sandoz 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": "20201206", "listing_expiration_date": "20261231"}