naloxone hydrochloride

Generic: naloxone hydrochloride nasal

Labeler: a-s medication solutions
NDC Directory HUMAN PRESCRIPTION DRUG NDA AUTHORIZED GENERIC Inactive Finished

Drug Facts

Product Profile

Brand Name naloxone hydrochloride
Generic Name naloxone hydrochloride nasal
Labeler a-s medication solutions
Dosage Form INHALANT
Routes
NASAL
Active Ingredients

naloxone hydrochloride 4 mg/.1mL

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-5908
Product ID 50090-5908_fefa320d-95d8-414e-ad54-40c9f6d2c55d
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA AUTHORIZED GENERIC
Application Number NDA208411
Listing Expiration 2026-12-31
Marketing Start 2021-12-20

Pharmacologic Class

Classes
opioid antagonist [epc] opioid antagonists [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500905908
Hyphenated Format 50090-5908

Supplemental Identifiers

RxCUI
1725059
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 nasal (source: ndc)
Application Number NDA208411 (source: ndc)
Routes
NASAL
source: ndc

Resolved Composition

Strengths
  • 4 mg/.1mL
source: ndc
Packaging
  • 2 VIAL, SINGLE-DOSE in 1 CARTON (50090-5908-0) / .1 mL in 1 VIAL, SINGLE-DOSE
source: ndc

Packages (1)

Ingredients (1)

naloxone hydrochloride (4 mg/.1mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["NASAL"], "spl_id": "fefa320d-95d8-414e-ad54-40c9f6d2c55d", "openfda": {"unii": ["F850569PQR"], "rxcui": ["1725059"], "spl_set_id": ["4517afa1-4b17-4a15-b91b-65b18bd0558f"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "2 VIAL, SINGLE-DOSE in 1 CARTON (50090-5908-0)  / .1 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "50090-5908-0", "marketing_start_date": "20220119"}], "brand_name": "Naloxone Hydrochloride", "product_id": "50090-5908_fefa320d-95d8-414e-ad54-40c9f6d2c55d", "dosage_form": "INHALANT", "pharm_class": ["Opioid Antagonist [EPC]", "Opioid Antagonists [MoA]"], "product_ndc": "50090-5908", "generic_name": "Naloxone Hydrochloride Nasal", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Naloxone Hydrochloride", "active_ingredients": [{"name": "NALOXONE HYDROCHLORIDE", "strength": "4 mg/.1mL"}], "application_number": "NDA208411", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20211220", "listing_expiration_date": "20261231"}