Package 0641-6132-25

Brand: naloxone hydrochloride

Generic: nalxone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0641-6132-25
Digits Only 0641613225
Product NDC 0641-6132
Product ID 0641-6132_4e1f7a9c-93dd-4e8e-b31d-ff9ea869995c
Description

25 VIAL in 1 CARTON (0641-6132-25) / 1 mL in 1 VIAL (0641-6132-01)

Marketing

Marketing Status
Marketed Since 1986-09-24
Brand naloxone hydrochloride
Generic nalxone 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": "4e1f7a9c-93dd-4e8e-b31d-ff9ea869995c", "openfda": {"unii": ["F850569PQR"], "rxcui": ["1659929"], "spl_set_id": ["8cc25cf1-008c-4808-baec-49f35a887fae"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 CARTON (0641-6132-25)  / 1 mL in 1 VIAL (0641-6132-01)", "package_ndc": "0641-6132-25", "marketing_start_date": "19860924"}], "brand_name": "Naloxone Hydrochloride", "product_id": "0641-6132_4e1f7a9c-93dd-4e8e-b31d-ff9ea869995c", "dosage_form": "INJECTION", "pharm_class": ["Opioid Antagonist [EPC]", "Opioid Antagonists [MoA]"], "product_ndc": "0641-6132", "generic_name": "Nalxone 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": "ANDA070299", "marketing_category": "ANDA", "marketing_start_date": "19860924", "listing_expiration_date": "20261231"}