naloxone hydrochloride
Generic: naloxone hydrochloride
Labeler: eugia us llcDrug Facts
Product Profile
Brand Name
naloxone hydrochloride
Generic Name
naloxone hydrochloride
Labeler
eugia us llc
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
naloxone hydrochloride 1 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
55150-345
Product ID
55150-345_6b48182a-4a21-4157-8efb-591ee87fb7d6
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA213279
Listing Expiration
2026-12-31
Marketing Start
2021-01-14
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
55150345
Hyphenated Format
55150-345
Supplemental Identifiers
RxCUI
UPC
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
naloxone hydrochloride (source: ndc)
Generic Name
naloxone hydrochloride (source: ndc)
Application Number
ANDA213279 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 1 mg/mL
Packaging
- 1 SYRINGE in 1 BOX (55150-345-01) / 2 mL in 1 SYRINGE
- 10 SYRINGE in 1 BOX (55150-345-10) / 2 mL in 1 SYRINGE
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS", "SUBCUTANEOUS"], "spl_id": "6b48182a-4a21-4157-8efb-591ee87fb7d6", "openfda": {"upc": ["0355150345014"], "unii": ["F850569PQR"], "rxcui": ["1191250"], "spl_set_id": ["8bcf426a-b4fc-4f24-9ad0-fb26168a0b56"], "manufacturer_name": ["Eugia US LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 SYRINGE in 1 BOX (55150-345-01) / 2 mL in 1 SYRINGE", "package_ndc": "55150-345-01", "marketing_start_date": "20210114"}, {"sample": false, "description": "10 SYRINGE in 1 BOX (55150-345-10) / 2 mL in 1 SYRINGE", "package_ndc": "55150-345-10", "marketing_start_date": "20210114"}], "brand_name": "Naloxone Hydrochloride", "product_id": "55150-345_6b48182a-4a21-4157-8efb-591ee87fb7d6", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Opioid Antagonist [EPC]", "Opioid Antagonists [MoA]"], "product_ndc": "55150-345", "generic_name": "Naloxone Hydrochloride", "labeler_name": "Eugia US LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Naloxone Hydrochloride", "active_ingredients": [{"name": "NALOXONE HYDROCHLORIDE", "strength": "1 mg/mL"}], "application_number": "ANDA213279", "marketing_category": "ANDA", "marketing_start_date": "20210114", "listing_expiration_date": "20261231"}