Package 71288-505-03
Brand: dexmedetomidine
Generic: dexmedetomidinePackage Facts
Identity
Package NDC
71288-505-03
Digits Only
7128850503
Product NDC
71288-505
Description
25 VIAL, SINGLE-DOSE in 1 CARTON (71288-505-03) / 2 mL in 1 VIAL, SINGLE-DOSE (71288-505-02)
Marketing
Marketing Status
Brand
dexmedetomidine
Generic
dexmedetomidine
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "74e25a75-2d63-4f39-b6d0-a73392bd1040", "openfda": {"unii": ["1018WH7F9I"], "rxcui": ["309710"], "spl_set_id": ["8fa36783-b94d-4084-8c41-40ee64192074"], "manufacturer_name": ["Meitheal Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL, SINGLE-DOSE in 1 CARTON (71288-505-03) / 2 mL in 1 VIAL, SINGLE-DOSE (71288-505-02)", "package_ndc": "71288-505-03", "marketing_start_date": "20190118"}], "brand_name": "DEXMEDETOMIDINE", "product_id": "71288-505_74e25a75-2d63-4f39-b6d0-a73392bd1040", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Adrenergic alpha2-Agonists [MoA]", "Central alpha-2 Adrenergic Agonist [EPC]", "General Anesthesia [PE]"], "product_ndc": "71288-505", "generic_name": "DEXMEDETOMIDINE", "labeler_name": "Meitheal Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "DEXMEDETOMIDINE", "active_ingredients": [{"name": "DEXMEDETOMIDINE HYDROCHLORIDE", "strength": "100 ug/mL"}], "application_number": "ANDA204843", "marketing_category": "ANDA", "marketing_start_date": "20190118", "listing_expiration_date": "20261231"}