naloxone hydrochloride

Generic: naloxone hydrochloride

Labeler: a-s medication solutions
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name naloxone hydrochloride
Generic Name naloxone hydrochloride
Labeler a-s medication solutions
Dosage Form INJECTION, SOLUTION
Routes
INTRAMUSCULAR INTRAVENOUS SUBCUTANEOUS
Active Ingredients

naloxone hydrochloride .4 mg/mL

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-6491
Product ID 50090-6491_139efb34-7bd4-46a7-9aeb-20e7b973d7a2
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA204997
Listing Expiration 2026-12-31
Marketing Start 2014-03-06

Pharmacologic Class

Classes
opioid antagonist [epc] opioid antagonists [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500906491
Hyphenated Format 50090-6491

Supplemental Identifiers

RxCUI
1659929
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 ANDA204997 (source: ndc)
Routes
INTRAMUSCULAR INTRAVENOUS SUBCUTANEOUS
source: ndc

Resolved Composition

Strengths
  • .4 mg/mL
source: ndc
Packaging
  • 10 VIAL, SINGLE-DOSE in 1 CARTON (50090-6491-0) / 1 mL in 1 VIAL, SINGLE-DOSE
source: ndc

Packages (1)

50090-6491-0 10 VIAL, SINGLE-DOSE in 1 CARTON (50090-6491-0) / 1 mL in 1 VIAL, SINGLE-DOSE

Ingredients (1)

naloxone hydrochloride (.4 mg/mL)

Linked Drug Pages (1)

Naloxone Hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAMUSCULAR", "INTRAVENOUS", "SUBCUTANEOUS"], "spl_id": "139efb34-7bd4-46a7-9aeb-20e7b973d7a2", "openfda": {"unii": ["F850569PQR"], "rxcui": ["1659929"], "spl_set_id": ["3d2dcee4-7510-477b-95a8-9b2afb773984"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL, SINGLE-DOSE in 1 CARTON (50090-6491-0)  / 1 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "50090-6491-0", "marketing_start_date": "20230519"}], "brand_name": "Naloxone Hydrochloride", "product_id": "50090-6491_139efb34-7bd4-46a7-9aeb-20e7b973d7a2", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Opioid Antagonist [EPC]", "Opioid Antagonists [MoA]"], "product_ndc": "50090-6491", "generic_name": "naloxone hydrochloride", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Naloxone Hydrochloride", "active_ingredients": [{"name": "NALOXONE HYDROCHLORIDE", "strength": ".4 mg/mL"}], "application_number": "ANDA204997", "marketing_category": "ANDA", "marketing_start_date": "20140306", "listing_expiration_date": "20261231"}