acetaminophen
Generic: acetaminophen
Labeler: solupharm pharmazeutische erzeugnisse gmbhDrug Facts
Product Profile
Brand Name
acetaminophen
Generic Name
acetaminophen
Labeler
solupharm pharmazeutische erzeugnisse gmbh
Dosage Form
INJECTION
Routes
Active Ingredients
acetaminophen 1000 mg/100mL
Manufacturer
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
UNII
Packaging Origin
Original Packager
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
source: ndc
Resolved Composition
Strengths
- 1000 mg/100mL
Packaging
- 24 BOTTLE in 1 BOTTLE (55579-110-01) / 100 mL in 1 BOTTLE
Packages (1)
Ingredients (1)
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"}