Package 72664-212-01
Brand: nadolol
Generic: nadololPackage Facts
Identity
Package NDC
72664-212-01
Digits Only
7266421201
Product NDC
72664-212
Description
100 TABLET in 1 BOTTLE, PLASTIC (72664-212-01)
Marketing
Marketing Status
Brand
nadolol
Generic
nadolol
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "05f81151-3c12-9235-e063-6294a90af890", "openfda": {"nui": ["N0000000161", "N0000175556"], "unii": ["FEN504330V"], "rxcui": ["198006", "198007", "198008"], "spl_set_id": ["85b4b931-51c4-4326-88ea-708dde8323d4"], "pharm_class_epc": ["beta-Adrenergic Blocker [EPC]"], "pharm_class_moa": ["Adrenergic beta-Antagonists [MoA]"], "manufacturer_name": ["VGYAAN Pharmaceuticals LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (72664-212-01)", "package_ndc": "72664-212-01", "marketing_start_date": "20200630"}], "brand_name": "NADOLOL", "product_id": "72664-212_05f81151-3c12-9235-e063-6294a90af890", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "72664-212", "generic_name": "NADOLOL", "labeler_name": "VGYAAN Pharmaceuticals LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "NADOLOL", "active_ingredients": [{"name": "NADOLOL", "strength": "40 mg/1"}], "application_number": "ANDA212856", "marketing_category": "ANDA", "marketing_start_date": "20200630", "listing_expiration_date": "20261231"}