Package 0409-1463-01

Brand: nalbuphine hydrochloride

Generic: nalbuphine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0409-1463-01
Digits Only 0409146301
Product NDC 0409-1463
Product ID 0409-1463_cbcbf107-67c0-4a8a-a25d-5a05c43a0bfd
Description

10 AMPULE in 1 TRAY (0409-1463-01) / 1 mL in 1 AMPULE (0409-1463-71)

Marketing

Marketing Status
Marketed Since 2005-03-31
Brand nalbuphine hydrochloride
Generic nalbuphine hydrochloride
Sample Package No

Linked Drug Pages (1)

Nalbuphine Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAMUSCULAR", "INTRAVENOUS", "SUBCUTANEOUS"], "spl_id": "cbcbf107-67c0-4a8a-a25d-5a05c43a0bfd", "openfda": {"unii": ["ZU4275277R"], "rxcui": ["904415", "904440", "1866543", "1866551"], "spl_set_id": ["6025e8d4-5083-4c3a-58a0-050e7b0b6150"], "manufacturer_name": ["Hospira, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 AMPULE in 1 TRAY (0409-1463-01)  / 1 mL in 1 AMPULE (0409-1463-71)", "package_ndc": "0409-1463-01", "marketing_start_date": "20050331"}], "brand_name": "Nalbuphine Hydrochloride", "product_id": "0409-1463_cbcbf107-67c0-4a8a-a25d-5a05c43a0bfd", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Competitive Opioid Antagonists [MoA]", "Opioid Agonist/Antagonist [EPC]", "Partial Opioid Agonists [MoA]"], "product_ndc": "0409-1463", "generic_name": "NALBUPHINE HYDROCHLORIDE", "labeler_name": "Hospira, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Nalbuphine Hydrochloride", "active_ingredients": [{"name": "NALBUPHINE HYDROCHLORIDE", "strength": "10 mg/mL"}], "application_number": "ANDA070914", "marketing_category": "ANDA", "marketing_start_date": "20050331", "listing_expiration_date": "20261231"}