Package 70069-071-10

Brand: naloxone hydrochloride

Generic: naloxone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70069-071-10
Digits Only 7006907110
Product NDC 70069-071
Product ID 70069-071_52551e7c-39ae-4d67-be09-97a5368ba6e4
Description

10 VIAL in 1 CARTON (70069-071-10) / 1 mL in 1 VIAL (70069-071-01)

Marketing

Marketing Status
Marketed Since 2017-08-08
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": "52551e7c-39ae-4d67-be09-97a5368ba6e4", "openfda": {"upc": ["0370069071014"], "unii": ["F850569PQR"], "rxcui": ["1659929"], "spl_set_id": ["dfa48492-d83b-48cc-9ad1-bdc0c2ac9931"], "manufacturer_name": ["Somerset Therapeutics, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL in 1 CARTON (70069-071-10)  / 1 mL in 1 VIAL (70069-071-01)", "package_ndc": "70069-071-10", "marketing_start_date": "20170808"}], "brand_name": "Naloxone Hydrochloride", "product_id": "70069-071_52551e7c-39ae-4d67-be09-97a5368ba6e4", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Opioid Antagonist [EPC]", "Opioid Antagonists [MoA]"], "product_ndc": "70069-071", "generic_name": "Naloxone Hydrochloride", "labeler_name": "Somerset Therapeutics, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Naloxone Hydrochloride", "active_ingredients": [{"name": "NALOXONE HYDROCHLORIDE", "strength": ".4 mg/mL"}], "application_number": "ANDA207633", "marketing_category": "ANDA", "marketing_start_date": "20170808", "listing_expiration_date": "20261231"}