Package 50090-5752-0

Brand: nebivolol

Generic: nebivolol
NDC Package

Package Facts

Identity

Package NDC 50090-5752-0
Digits Only 5009057520
Product NDC 50090-5752
Product ID 50090-5752_b7236465-ffd4-4834-8f62-227246ac4961
Description

30 TABLET in 1 BOTTLE (50090-5752-0)

Marketing

Marketing Status
Marketed Since 2021-09-30
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": "b7236465-ffd4-4834-8f62-227246ac4961", "openfda": {"unii": ["JGS34J7L9I"], "rxcui": ["387013"], "spl_set_id": ["f85d7b19-51d9-47d9-bd7b-13d45ad7759b"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (50090-5752-0)", "package_ndc": "50090-5752-0", "marketing_start_date": "20210930"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-5752-1)", "package_ndc": "50090-5752-1", "marketing_start_date": "20210930"}], "brand_name": "Nebivolol", "product_id": "50090-5752_b7236465-ffd4-4834-8f62-227246ac4961", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "50090-5752", "generic_name": "Nebivolol", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Nebivolol", "active_ingredients": [{"name": "NEBIVOLOL HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA203828", "marketing_category": "ANDA", "marketing_start_date": "20210916", "listing_expiration_date": "20271231"}