acetaminophen

Generic: acetaminophen

Labeler: solupharm pharmazeutische erzeugnisse gmbh
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name acetaminophen
Generic Name acetaminophen
Labeler solupharm pharmazeutische erzeugnisse gmbh
Dosage Form INJECTION
Routes
INTRAVENOUS
Active Ingredients

acetaminophen 1000 mg/100mL

Manufacturer
Solupharm Pharmazeutische Erzeugnisse GmbH

Identifiers & Regulatory

Product NDC 55579-110
Product ID 55579-110_f49c61bc-9a3e-d885-e053-2995a90ad8af
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA202605
Listing Expiration 2026-12-31
Marketing Start 2020-12-07

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 55579110
Hyphenated Format 55579-110

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
  • 1000 mg/100mL
source: ndc
Packaging
  • 24 BOTTLE in 1 BOTTLE (55579-110-01) / 100 mL in 1 BOTTLE
source: ndc

Packages (1)

Ingredients (1)

acetaminophen (1000 mg/100mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "f49c61bc-9a3e-d885-e053-2995a90ad8af", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["483017"], "spl_set_id": ["adeebc6c-c82f-40dc-b813-1b02244984ce"], "manufacturer_name": ["Solupharm Pharmazeutische Erzeugnisse GmbH"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "24 BOTTLE in 1 BOTTLE (55579-110-01)  / 100 mL in 1 BOTTLE", "package_ndc": "55579-110-01", "marketing_start_date": "20230301"}], "brand_name": "Acetaminophen", "product_id": "55579-110_f49c61bc-9a3e-d885-e053-2995a90ad8af", "dosage_form": "INJECTION", "product_ndc": "55579-110", "generic_name": "ACETAMINOPHEN", "labeler_name": "Solupharm Pharmazeutische Erzeugnisse GmbH", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Acetaminophen", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "1000 mg/100mL"}], "application_number": "ANDA202605", "marketing_category": "ANDA", "marketing_start_date": "20201207", "listing_expiration_date": "20261231"}