Package 68001-630-00

Brand: nadolol

Generic: nadolol
NDC Package

Package Facts

Identity

Package NDC 68001-630-00
Digits Only 6800163000
Product NDC 68001-630
Description

100 TABLET in 1 BOTTLE (68001-630-00)

Marketing

Marketing Status
Marketed Since 2025-03-01
Brand nadolol
Generic nadolol
Sample Package No

Linked Drug Pages (0)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "32599062-2d4b-2ba7-e063-6394a90a05f0", "openfda": {"nui": ["N0000000161", "N0000175556"], "unii": ["FEN504330V"], "rxcui": ["198006", "198007", "198008"], "spl_set_id": ["15822faf-6924-4a63-a4e1-6058b308708c"], "pharm_class_epc": ["beta-Adrenergic Blocker [EPC]"], "pharm_class_moa": ["Adrenergic beta-Antagonists [MoA]"], "manufacturer_name": ["BluePoint Laboratories"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (68001-630-00)", "package_ndc": "68001-630-00", "marketing_start_date": "20250301"}], "brand_name": "Nadolol", "product_id": "68001-630_32599062-2d4b-2ba7-e063-6394a90a05f0", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "68001-630", "generic_name": "Nadolol", "labeler_name": "BluePoint Laboratories", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Nadolol", "active_ingredients": [{"name": "NADOLOL", "strength": "20 mg/1"}], "application_number": "ANDA210955", "marketing_category": "ANDA", "marketing_start_date": "20250107", "listing_expiration_date": "20261231"}