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 80 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 71335-2131
Product ID 71335-2131_8f92e29a-0df8-4331-8788-bc126ef424f9
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA210955
Listing Expiration 2026-12-31
Marketing Start 2019-07-26

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 713352131
Hyphenated Format 71335-2131

Supplemental Identifiers

RxCUI
198008
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 ANDA210955 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 80 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (71335-2131-1)
  • 28 TABLET in 1 BOTTLE (71335-2131-2)
  • 90 TABLET in 1 BOTTLE (71335-2131-3)
source: ndc

Packages (3)

Ingredients (1)

nadolol (80 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "8f92e29a-0df8-4331-8788-bc126ef424f9", "openfda": {"nui": ["N0000000161", "N0000175556"], "unii": ["FEN504330V"], "rxcui": ["198008"], "spl_set_id": ["c154d99c-e4fb-41d0-8fac-e1982672e8d7"], "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": "30 TABLET in 1 BOTTLE (71335-2131-1)", "package_ndc": "71335-2131-1", "marketing_start_date": "20220719"}, {"sample": false, "description": "28 TABLET in 1 BOTTLE (71335-2131-2)", "package_ndc": "71335-2131-2", "marketing_start_date": "20240403"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71335-2131-3)", "package_ndc": "71335-2131-3", "marketing_start_date": "20240403"}], "brand_name": "Nadolol", "product_id": "71335-2131_8f92e29a-0df8-4331-8788-bc126ef424f9", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "71335-2131", "generic_name": "Nadolol", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Nadolol", "active_ingredients": [{"name": "NADOLOL", "strength": "80 mg/1"}], "application_number": "ANDA210955", "marketing_category": "ANDA", "marketing_start_date": "20190726", "listing_expiration_date": "20261231"}