naloxone hydrochloride

Generic: naloxone hydrochloride

Labeler: henry schein, inc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

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

Manufacturer
Henry Schein, Inc

Identifiers & Regulatory

Product NDC 0404-9922
Product ID 0404-9922_ace20fdd-3422-48d9-acf4-da37f78f13a7
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA072076
Listing Expiration 2027-12-31
Marketing Start 2022-01-13

Pharmacologic Class

Classes
opioid antagonist [epc] opioid antagonists [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 04049922
Hyphenated Format 0404-9922

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 (0404-9922-02) / 2 mL in 1 SYRINGE
source: ndc

Packages (1)

0404-9922-02 1 SYRINGE in 1 BAG (0404-9922-02) / 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": "ace20fdd-3422-48d9-acf4-da37f78f13a7", "openfda": {"unii": ["F850569PQR"], "rxcui": ["1191250"], "spl_set_id": ["bd65e3fe-cd7a-4855-8f55-8cc3a0921ccc"], "manufacturer_name": ["Henry Schein, Inc"]}, "finished": true, "packaging": [{"sample": false, "description": "1 SYRINGE in 1 BAG (0404-9922-02)  / 2 mL in 1 SYRINGE", "package_ndc": "0404-9922-02", "marketing_start_date": "20220113"}], "brand_name": "NALOXONE HYDROCHLORIDE", "product_id": "0404-9922_ace20fdd-3422-48d9-acf4-da37f78f13a7", "dosage_form": "INJECTION", "pharm_class": ["Opioid Antagonist [EPC]", "Opioid Antagonists [MoA]"], "product_ndc": "0404-9922", "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_start_date": "20220113", "listing_expiration_date": "20271231"}