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
Routes
PARENTERAL
Active Ingredients

naloxone hydrochloride 1 mg/mL

Manufacturer
Medical Purchasing Solutions, LLC

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
opioid antagonist [epc] opioid antagonists [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 718727177
Hyphenated Format 71872-7177

Supplemental Identifiers

RxCUI
1191250
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 ANDA072076 (source: ndc)
Routes
PARENTERAL
source: ndc

Resolved Composition

Strengths
  • 1 mg/mL
source: ndc
Packaging
  • 1 SYRINGE in 1 BAG (71872-7177-1) / 2 mL in 1 SYRINGE
source: ndc

Packages (1)

Ingredients (1)

naloxone hydrochloride (1 mg/mL)

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"}