Package 70069-661-10

Brand: nalbuphine hydrochloride

Generic: nalbuphine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70069-661-10
Digits Only 7006966110
Product NDC 70069-661
Product ID 70069-661_d4c32b91-24cf-43f2-a1d2-0120f31bbba8
Description

1 VIAL, MULTI-DOSE in 1 CARTON (70069-661-10) / 10 mL in 1 VIAL, MULTI-DOSE

Marketing

Marketing Status
Marketed Since 2024-09-26
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": "d4c32b91-24cf-43f2-a1d2-0120f31bbba8", "openfda": {"upc": ["0370069661017", "0370069662014"], "unii": ["ZU4275277R"], "rxcui": ["904415", "904440"], "spl_set_id": ["d82dafac-cce7-445a-8127-2a10b6d947ca"], "manufacturer_name": ["Somerset Therapeutics, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, MULTI-DOSE in 1 CARTON (70069-661-10)  / 10 mL in 1 VIAL, MULTI-DOSE", "package_ndc": "70069-661-10", "marketing_start_date": "20240926"}], "brand_name": "Nalbuphine hydrochloride", "product_id": "70069-661_d4c32b91-24cf-43f2-a1d2-0120f31bbba8", "dosage_form": "INJECTION", "pharm_class": ["Competitive Opioid Antagonists [MoA]", "Opioid Agonist/Antagonist [EPC]", "Partial Opioid Agonists [MoA]"], "product_ndc": "70069-661", "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": "10 mg/mL"}], "application_number": "ANDA216049", "marketing_category": "ANDA", "marketing_start_date": "20240926", "listing_expiration_date": "20261231"}