naloxone hydrochloride
Generic: naloxone hydrochloride
Labeler: medical purchasing solutions, llcDrug Facts
Product Profile
Brand Name
naloxone hydrochloride
Generic Name
naloxone hydrochloride
Labeler
medical purchasing solutions, llc
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
naloxone hydrochloride .4 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
71872-7326
Product ID
71872-7326_28f3d32d-b65b-5c4c-e063-6394a90ae561
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA207634
Listing Expiration
2026-12-31
Marketing Start
2017-07-26
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
718727326
Hyphenated Format
71872-7326
Supplemental Identifiers
RxCUI
UPC
UNII
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
ANDA207634 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- .4 mg/mL
Packaging
- 1 CARTON in 1 BAG (71872-7326-1) / 1 VIAL, GLASS in 1 CARTON / 10 mL in 1 VIAL, GLASS
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS", "SUBCUTANEOUS"], "spl_id": "28f3d32d-b65b-5c4c-e063-6394a90ae561", "openfda": {"upc": ["0370069072011"], "unii": ["F850569PQR"], "rxcui": ["1191222"], "spl_set_id": ["28f3e3bc-b1be-9f06-e063-6394a90a1936"], "manufacturer_name": ["Medical Purchasing Solutions, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "1 CARTON in 1 BAG (71872-7326-1) / 1 VIAL, GLASS in 1 CARTON / 10 mL in 1 VIAL, GLASS", "package_ndc": "71872-7326-1", "marketing_start_date": "20240619"}], "brand_name": "Naloxone Hydrochloride", "product_id": "71872-7326_28f3d32d-b65b-5c4c-e063-6394a90ae561", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Opioid Antagonist [EPC]", "Opioid Antagonists [MoA]"], "product_ndc": "71872-7326", "generic_name": "Naloxone Hydrochloride", "labeler_name": "Medical Purchasing Solutions, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Naloxone Hydrochloride", "active_ingredients": [{"name": "NALOXONE HYDROCHLORIDE", "strength": ".4 mg/mL"}], "application_number": "ANDA207634", "marketing_category": "ANDA", "marketing_start_date": "20170726", "listing_expiration_date": "20261231"}