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
Routes
Active Ingredients
naloxone hydrochloride 1 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
71872-7177
Product ID
71872-7177_fbbce2ae-1daa-b037-e053-6394a90a3397
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA072076
Listing Expiration
2026-12-31
Marketing Start
2001-06-01
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
718727177
Hyphenated Format
71872-7177
Supplemental Identifiers
RxCUI
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
ANDA072076 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 1 mg/mL
Packaging
- 1 SYRINGE in 1 BAG (71872-7177-1) / 2 mL in 1 SYRINGE
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["PARENTERAL"], "spl_id": "fbbce2ae-1daa-b037-e053-6394a90a3397", "openfda": {"unii": ["F850569PQR"], "rxcui": ["1191250"], "spl_set_id": ["958577c3-d2c4-26ad-e053-2a95a90ad73a"], "manufacturer_name": ["Medical Purchasing Solutions, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "1 SYRINGE in 1 BAG (71872-7177-1) / 2 mL in 1 SYRINGE", "package_ndc": "71872-7177-1", "marketing_start_date": "20190909"}], "brand_name": "Naloxone Hydrochloride", "product_id": "71872-7177_fbbce2ae-1daa-b037-e053-6394a90a3397", "dosage_form": "INJECTION", "pharm_class": ["Opioid Antagonist [EPC]", "Opioid Antagonists [MoA]"], "product_ndc": "71872-7177", "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": "1 mg/mL"}], "application_number": "ANDA072076", "marketing_category": "ANDA", "marketing_start_date": "20010601", "listing_expiration_date": "20261231"}