nadolol

Generic: nadolol

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name nadolol
Generic Name nadolol
Labeler bryant ranch prepack
Dosage Form TABLET
Routes
ORAL
Active Ingredients

nadolol 20 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 72162-2234
Product ID 72162-2234_14d427a2-ac49-4805-95c2-79e3151ea616
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA203455
Listing Expiration 2026-12-31
Marketing Start 2016-02-23

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 721622234
Hyphenated Format 72162-2234

Supplemental Identifiers

RxCUI
198006
UNII
FEN504330V
NUI
N0000000161 N0000175556

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 ANDA203455 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (72162-2234-1)
source: ndc

Packages (1)

Ingredients (1)

nadolol (20 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "14d427a2-ac49-4805-95c2-79e3151ea616", "openfda": {"nui": ["N0000000161", "N0000175556"], "unii": ["FEN504330V"], "rxcui": ["198006"], "spl_set_id": ["2fc1f850-9653-4082-929a-926b644810e7"], "pharm_class_epc": ["beta-Adrenergic Blocker [EPC]"], "pharm_class_moa": ["Adrenergic beta-Antagonists [MoA]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (72162-2234-1)", "package_ndc": "72162-2234-1", "marketing_start_date": "20240126"}], "brand_name": "Nadolol", "product_id": "72162-2234_14d427a2-ac49-4805-95c2-79e3151ea616", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "72162-2234", "generic_name": "Nadolol", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Nadolol", "active_ingredients": [{"name": "NADOLOL", "strength": "20 mg/1"}], "application_number": "ANDA203455", "marketing_category": "ANDA", "marketing_start_date": "20160223", "listing_expiration_date": "20261231"}