Package 51662-1420-1
Brand: nalbuphine hci
Generic: nalbuphine hciPackage Facts
Identity
Package NDC
51662-1420-1
Digits Only
5166214201
Product NDC
51662-1420
Description
1 VIAL, MULTI-DOSE in 1 CARTON (51662-1420-1) / 10 mL in 1 VIAL, MULTI-DOSE
Marketing
Marketing Status
Brand
nalbuphine hci
Generic
nalbuphine hci
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS", "SUBCUTANEOUS"], "spl_id": "2b37c789-d5da-dc83-e063-6294a90a4ca5", "openfda": {"unii": ["ZU4275277R"], "rxcui": ["904415"], "spl_set_id": ["96139914-0708-7b58-e053-2995a90a7308"], "manufacturer_name": ["HF Acquisition Co LLC, DBA HealthFirst"]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, MULTI-DOSE in 1 CARTON (51662-1420-1) / 10 mL in 1 VIAL, MULTI-DOSE", "package_ndc": "51662-1420-1", "marketing_start_date": "20191029"}], "brand_name": "NALBUPHINE HCI", "product_id": "51662-1420_2b37c789-d5da-dc83-e063-6294a90a4ca5", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Competitive Opioid Antagonists [MoA]", "Opioid Agonist/Antagonist [EPC]", "Partial Opioid Agonists [MoA]"], "product_ndc": "51662-1420", "generic_name": "NALBUPHINE HCI", "labeler_name": "HF Acquisition Co LLC, DBA HealthFirst", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "NALBUPHINE HCI", "active_ingredients": [{"name": "NALBUPHINE HYDROCHLORIDE", "strength": "10 mg/mL"}], "application_number": "ANDA070915", "marketing_category": "ANDA", "marketing_start_date": "20191029", "listing_expiration_date": "20261231"}