Package 0641-6193-10

Brand: naloxone hydrochloride

Generic: naloxone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0641-6193-10
Digits Only 0641619310
Product NDC 0641-6193
Product ID 0641-6193_2f3fbff5-628a-49f6-9867-06c876742876
Description

10 SYRINGE in 1 CARTON (0641-6193-10) / 1 mL in 1 SYRINGE (0641-6193-01)

Marketing

Marketing Status
Marketed Since 2025-08-31
Brand naloxone hydrochloride
Generic naloxone hydrochloride
Sample Package No

Linked Drug Pages (1)

Naloxone Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAMUSCULAR", "INTRAVENOUS", "SUBCUTANEOUS"], "spl_id": "2f3fbff5-628a-49f6-9867-06c876742876", "openfda": {"unii": ["F850569PQR"], "rxcui": ["1191250", "2679504"], "spl_set_id": ["e6467385-6990-498c-8a0e-f4a40ef33cb7"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 SYRINGE in 1 CARTON (0641-6193-10)  / 1 mL in 1 SYRINGE (0641-6193-01)", "package_ndc": "0641-6193-10", "marketing_start_date": "20250831"}], "brand_name": "Naloxone Hydrochloride", "product_id": "0641-6193_2f3fbff5-628a-49f6-9867-06c876742876", "dosage_form": "INJECTION", "pharm_class": ["Opioid Antagonist [EPC]", "Opioid Antagonists [MoA]"], "product_ndc": "0641-6193", "generic_name": "Naloxone Hydrochloride", "labeler_name": "Hikma Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Naloxone Hydrochloride", "active_ingredients": [{"name": "NALOXONE HYDROCHLORIDE", "strength": ".4 mg/mL"}], "application_number": "ANDA212300", "marketing_category": "ANDA", "marketing_start_date": "20250725", "listing_expiration_date": "20261231"}