Package 67877-390-90

Brand: nebivolol

Generic: nebivolol
NDC Package

Package Facts

Identity

Package NDC 67877-390-90
Digits Only 6787739090
Product NDC 67877-390
Description

90 TABLET in 1 BOTTLE (67877-390-90)

Marketing

Marketing Status
Marketed Since 2021-09-16
Brand nebivolol
Generic nebivolol
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4f315a54-2598-4463-8884-0b643e86f8c0", "openfda": {"upc": ["0367877393308", "0367877391304", "0367877392905", "0367877390901"], "unii": ["JGS34J7L9I"], "rxcui": ["387013", "751612", "751618", "827073"], "spl_set_id": ["fecef8fc-b66b-4133-b66f-8d6b72750622"], "manufacturer_name": ["Ascend Laboratories, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (67877-390-01)", "package_ndc": "67877-390-01", "marketing_start_date": "20210916"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (67877-390-30)", "package_ndc": "67877-390-30", "marketing_start_date": "20210916"}, {"sample": false, "description": "1 BLISTER PACK in 1 CARTON (67877-390-33)  / 10 TABLET in 1 BLISTER PACK", "package_ndc": "67877-390-33", "marketing_start_date": "20210916"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (67877-390-90)", "package_ndc": "67877-390-90", "marketing_start_date": "20210916"}], "brand_name": "Nebivolol", "product_id": "67877-390_4f315a54-2598-4463-8884-0b643e86f8c0", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "67877-390", "generic_name": "Nebivolol", "labeler_name": "Ascend Laboratories, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Nebivolol", "active_ingredients": [{"name": "NEBIVOLOL HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA203828", "marketing_category": "ANDA", "marketing_start_date": "20210916", "listing_expiration_date": "20261231"}