Package 0904-7499-04
Brand: nebivolol
Generic: nebivololPackage Facts
Identity
Package NDC
0904-7499-04
Digits Only
0904749904
Product NDC
0904-7499
Description
30 BLISTER PACK in 1 CARTON (0904-7499-04) / 1 TABLET in 1 BLISTER PACK
Marketing
Marketing Status
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": "d4d0a3fd-6520-4358-acce-8ecb76bfd8f7", "openfda": {"nui": ["N0000000161", "N0000175556"], "unii": ["030Y90569U"], "rxcui": ["387013", "751612", "751618"], "spl_set_id": ["3e9e1048-b5ea-4d6a-9363-3ee0d059e088"], "pharm_class_epc": ["beta-Adrenergic Blocker [EPC]"], "pharm_class_moa": ["Adrenergic beta-Antagonists [MoA]"], "manufacturer_name": ["Major Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "30 BLISTER PACK in 1 CARTON (0904-7499-04) / 1 TABLET in 1 BLISTER PACK", "package_ndc": "0904-7499-04", "marketing_start_date": "20250224"}], "brand_name": "NEBIVOLOL", "product_id": "0904-7499_d4d0a3fd-6520-4358-acce-8ecb76bfd8f7", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "0904-7499", "generic_name": "nebivolol", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "NEBIVOLOL", "active_ingredients": [{"name": "NEBIVOLOL", "strength": "10 mg/1"}], "application_number": "ANDA212682", "marketing_category": "ANDA", "marketing_start_date": "20250224", "listing_expiration_date": "20261231"}