Package 70069-672-10

Brand: nalbuphine hydrochloride

Generic: nalbuphine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70069-672-10
Digits Only 7006967210
Product NDC 70069-672
Product ID 70069-672_d7e3d7be-ce38-4696-979c-64dd1023a4cd
Description

10 AMPULE in 1 CARTON (70069-672-10) / 1 mL in 1 AMPULE (70069-672-01)

Marketing

Marketing Status
Marketed Since 2024-09-25
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": "d7e3d7be-ce38-4696-979c-64dd1023a4cd", "openfda": {"upc": ["0370069671108", "0370069671016", "0370069672013", "0370069672105"], "unii": ["ZU4275277R"], "rxcui": ["1866543", "1866551"], "spl_set_id": ["a3221c05-5822-4ab8-b589-0e3939b91a68"], "manufacturer_name": ["Somerset Therapeutics, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 AMPULE in 1 CARTON (70069-672-10)  / 1 mL in 1 AMPULE (70069-672-01)", "package_ndc": "70069-672-10", "marketing_start_date": "20240925"}], "brand_name": "Nalbuphine hydrochloride", "product_id": "70069-672_d7e3d7be-ce38-4696-979c-64dd1023a4cd", "dosage_form": "INJECTION", "pharm_class": ["Competitive Opioid Antagonists [MoA]", "Opioid Agonist/Antagonist [EPC]", "Partial Opioid Agonists [MoA]"], "product_ndc": "70069-672", "generic_name": "Nalbuphine hydrochloride", "labeler_name": "Somerset Therapeutics, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Nalbuphine hydrochloride", "active_ingredients": [{"name": "NALBUPHINE HYDROCHLORIDE", "strength": "20 mg/mL"}], "application_number": "ANDA216050", "marketing_category": "ANDA", "marketing_start_date": "20240925", "listing_expiration_date": "20261231"}