NALOXONE HYDROCHLORIDE

Generic: naloxone hydrochloride

Labeler: Henry Schein, Inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive

Drug Facts

Product Profile

Brand Name NALOXONE HYDROCHLORIDE
Generic Name naloxone hydrochloride
Labeler Henry Schein, Inc.
Dosage Form INJECTION
Routes
PARENTERAL
Active Ingredients

NALOXONE HYDROCHLORIDE 1 mg/mL

Identifiers & Regulatory

Product NDC 0404-9921
Product ID 0404-9921_08021e60-380c-4a63-a943-00b3dec83ced
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA072076
Marketing Start 2022-01-18
Marketing End 2026-02-28

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 04049921
Hyphenated Format 0404-9921

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 BOX in 1 BAG (0404-9921-02) / 1 SYRINGE in 1 BOX / 2 mL in 1 SYRINGE
source: ndc

Packages (1)

0404-9921-02 1 BOX in 1 BAG (0404-9921-02) / 1 SYRINGE in 1 BOX / 2 mL in 1 SYRINGE

Ingredients (1)

NALOXONE HYDROCHLORIDE (1 mg/mL)

Linked Drug Pages (1)

NALOXONE HYDROCHLORIDE ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["PARENTERAL"], "spl_id": "08021e60-380c-4a63-a943-00b3dec83ced", "openfda": {"unii": ["F850569PQR"], "rxcui": ["1191250"], "spl_set_id": ["6d8e0730-f224-4186-9927-6acce7d3392b"], "manufacturer_name": ["Henry Schein, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOX in 1 BAG (0404-9921-02)  / 1 SYRINGE in 1 BOX / 2 mL in 1 SYRINGE", "package_ndc": "0404-9921-02", "marketing_end_date": "20260228", "marketing_start_date": "20220118"}], "brand_name": "NALOXONE HYDROCHLORIDE", "product_id": "0404-9921_08021e60-380c-4a63-a943-00b3dec83ced", "dosage_form": "INJECTION", "pharm_class": ["Opioid Antagonist [EPC]", "Opioid Antagonists [MoA]"], "product_ndc": "0404-9921", "generic_name": "naloxone hydrochloride", "labeler_name": "Henry Schein, Inc.", "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_end_date": "20260228", "marketing_start_date": "20220118"}