naloxone hydrochloride

Generic: naloxone hydrochloride

Labeler: medical purchasing solutions, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name naloxone hydrochloride
Generic Name naloxone hydrochloride
Labeler medical purchasing solutions, llc
Dosage Form INJECTION, SOLUTION
Routes
INTRAMUSCULAR INTRAVENOUS SUBCUTANEOUS
Active Ingredients

naloxone hydrochloride .4 mg/mL

Manufacturer
Medical Purchasing Solutions, LLC

Identifiers & Regulatory

Product NDC 71872-7215
Product ID 71872-7215_facf199d-f6dd-926f-e053-6294a90ad1ee
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA212456
Listing Expiration 2026-12-31
Marketing Start 2019-11-04

Pharmacologic Class

Classes
opioid antagonist [epc] opioid antagonists [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 718727215
Hyphenated Format 71872-7215

Supplemental Identifiers

RxCUI
1191222
UNII
F850569PQR

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 ANDA212456 (source: ndc)
Routes
INTRAMUSCULAR INTRAVENOUS SUBCUTANEOUS
source: ndc

Resolved Composition

Strengths
  • .4 mg/mL
source: ndc
Packaging
  • 1 VIAL, MULTI-DOSE in 1 BAG (71872-7215-1) / 10 mL in 1 VIAL, MULTI-DOSE
source: ndc

Packages (1)

71872-7215-1 1 VIAL, MULTI-DOSE in 1 BAG (71872-7215-1) / 10 mL in 1 VIAL, MULTI-DOSE

Ingredients (1)

naloxone hydrochloride (.4 mg/mL)

Linked Drug Pages (1)

NALOXONE HYDROCHLORIDE ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAMUSCULAR", "INTRAVENOUS", "SUBCUTANEOUS"], "spl_id": "facf199d-f6dd-926f-e053-6294a90ad1ee", "openfda": {"unii": ["F850569PQR"], "rxcui": ["1191222"], "spl_set_id": ["ada6856c-5293-fc2f-e053-2995a90a8ec6"], "manufacturer_name": ["Medical Purchasing Solutions, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, MULTI-DOSE in 1 BAG (71872-7215-1)  / 10 mL in 1 VIAL, MULTI-DOSE", "package_ndc": "71872-7215-1", "marketing_start_date": "20200615"}], "brand_name": "NALOXONE HYDROCHLORIDE", "product_id": "71872-7215_facf199d-f6dd-926f-e053-6294a90ad1ee", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Opioid Antagonist [EPC]", "Opioid Antagonists [MoA]"], "product_ndc": "71872-7215", "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": "ANDA212456", "marketing_category": "ANDA", "marketing_start_date": "20191104", "listing_expiration_date": "20261231"}