nadolol

Generic: nadolol

Labeler: aurobindo pharma limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name nadolol
Generic Name nadolol
Labeler aurobindo pharma limited
Dosage Form TABLET
Routes
ORAL
Active Ingredients

nadolol 20 mg/1

Manufacturer
Aurobindo Pharma Limited

Identifiers & Regulatory

Product NDC 59651-589
Product ID 59651-589_bfed393e-1baf-439a-8073-998c1a97b276
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA201893
Listing Expiration 2026-12-31
Marketing Start 2022-06-07

Pharmacologic Class

Established (EPC)
beta-adrenergic blocker [epc]
Mechanism of Action
adrenergic beta-antagonists [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 59651589
Hyphenated Format 59651-589

Supplemental Identifiers

RxCUI
198006 198007 198008
UNII
FEN504330V
NUI
N0000000161 N0000175556

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name nadolol (source: ndc)
Generic Name nadolol (source: ndc)
Application Number ANDA201893 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (59651-589-01)
source: ndc

Packages (1)

59651-589-01 100 TABLET in 1 BOTTLE (59651-589-01)

Ingredients (1)

nadolol (20 mg/1)

Linked Drug Pages (1)

Nadolol ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "bfed393e-1baf-439a-8073-998c1a97b276", "openfda": {"nui": ["N0000000161", "N0000175556"], "unii": ["FEN504330V"], "rxcui": ["198006", "198007", "198008"], "spl_set_id": ["44c5352d-89f8-4bd3-9479-1069304562ca"], "pharm_class_epc": ["beta-Adrenergic Blocker [EPC]"], "pharm_class_moa": ["Adrenergic beta-Antagonists [MoA]"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (59651-589-01)", "package_ndc": "59651-589-01", "marketing_start_date": "20220607"}], "brand_name": "Nadolol", "product_id": "59651-589_bfed393e-1baf-439a-8073-998c1a97b276", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "59651-589", "generic_name": "Nadolol", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Nadolol", "active_ingredients": [{"name": "NADOLOL", "strength": "20 mg/1"}], "application_number": "ANDA201893", "marketing_category": "ANDA", "marketing_start_date": "20220607", "listing_expiration_date": "20261231"}