Package 68462-618-01

Brand: nebivolol

Generic: nebivolol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68462-618-01
Digits Only 6846261801
Product NDC 68462-618
Description

100 TABLET in 1 BOTTLE (68462-618-01)

Marketing

Marketing Status
Marketed Since 2017-05-25
Brand nebivolol
Generic nebivolol hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "151f00ae-13ed-4174-bf4d-bc30f1fb9d69", "openfda": {"upc": ["0368462618011", "0368462617014", "0368462615010", "0368462616017"], "unii": ["JGS34J7L9I"], "rxcui": ["387013", "751612", "751618", "827073"], "spl_set_id": ["cb47560d-9e35-4b0f-b12b-6ea478684a5b"], "manufacturer_name": ["Glenmark Pharmaceuticals Inc., USA"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (68462-618-01)", "package_ndc": "68462-618-01", "marketing_start_date": "20170525"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (68462-618-11)  / 10 TABLET in 1 BLISTER PACK", "package_ndc": "68462-618-11", "marketing_start_date": "20170525"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (68462-618-30)", "package_ndc": "68462-618-30", "marketing_start_date": "20170525"}], "brand_name": "nebivolol", "product_id": "68462-618_151f00ae-13ed-4174-bf4d-bc30f1fb9d69", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "68462-618", "generic_name": "nebivolol hydrochloride", "labeler_name": "Glenmark Pharmaceuticals Inc., USA", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "nebivolol", "active_ingredients": [{"name": "NEBIVOLOL HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA203821", "marketing_category": "ANDA", "marketing_start_date": "20170525", "listing_expiration_date": "20261231"}