naloxone hydrochloride
Generic: naloxone hydrochloride nasal
Labeler: a-s medication solutionsDrug Facts
Product Profile
Brand Name
naloxone hydrochloride
Generic Name
naloxone hydrochloride nasal
Labeler
a-s medication solutions
Dosage Form
INHALANT
Routes
Active Ingredients
naloxone hydrochloride 4 mg/.1mL
Manufacturer
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
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
500905908
Hyphenated Format
50090-5908
Supplemental Identifiers
RxCUI
UNII
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
source: ndc
Resolved Composition
Strengths
- 4 mg/.1mL
Packaging
- 2 VIAL, SINGLE-DOSE in 1 CARTON (50090-5908-0) / .1 mL in 1 VIAL, SINGLE-DOSE
Packages (1)
Ingredients (1)
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"}