Package 50090-5708-1

Brand: nebivolol

Generic: nebivolol
NDC Package

Package Facts

Identity

Package NDC 50090-5708-1
Digits Only 5009057081
Product NDC 50090-5708
Product ID 50090-5708_980722af-2bc3-492d-a8ff-835f3b69dd19
Description

90 TABLET in 1 BOTTLE (50090-5708-1)

Marketing

Marketing Status
Marketed Since 2021-10-07
Brand nebivolol
Generic nebivolol
Sample Package No

Linked Drug Pages (1)

Nebivolol ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "980722af-2bc3-492d-a8ff-835f3b69dd19", "openfda": {"unii": ["JGS34J7L9I"], "rxcui": ["751618"], "spl_set_id": ["5953f23b-2f41-4b49-bcdb-1691f4ffa35f"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "5 TABLET in 1 BOTTLE (50090-5708-0)", "package_ndc": "50090-5708-0", "marketing_start_date": "20210923"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-5708-1)", "package_ndc": "50090-5708-1", "marketing_start_date": "20211007"}], "brand_name": "Nebivolol", "product_id": "50090-5708_980722af-2bc3-492d-a8ff-835f3b69dd19", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "50090-5708", "generic_name": "Nebivolol", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Nebivolol", "active_ingredients": [{"name": "NEBIVOLOL HYDROCHLORIDE", "strength": "2.5 mg/1"}], "application_number": "ANDA203828", "marketing_category": "ANDA", "marketing_start_date": "20210916", "listing_expiration_date": "20261231"}