nadolol

Generic: nadolol

Labeler: bluepoint laboratories
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name nadolol
Generic Name nadolol
Labeler bluepoint laboratories
Dosage Form TABLET
Routes
ORAL
Active Ingredients

nadolol 20 mg/1

Manufacturer
BluePoint Laboratories

Identifiers & Regulatory

Product NDC 68001-317
Product ID 68001-317_1980a55f-434f-5c45-e063-6394a90a014e
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 68001317
Hyphenated Format 68001-317

Supplemental Identifiers

RxCUI
198006 198007 198008
UPC
0368001319003 0368001317009 0368001318006
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 ANDA203455 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (68001-317-00)
source: ndc

Packages (1)

68001-317-00 100 TABLET in 1 BOTTLE (68001-317-00)

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": "1980a55f-434f-5c45-e063-6394a90a014e", "openfda": {"nui": ["N0000000161", "N0000175556"], "upc": ["0368001319003", "0368001317009", "0368001318006"], "unii": ["FEN504330V"], "rxcui": ["198006", "198007", "198008"], "spl_set_id": ["0a2acdc0-aab6-462e-a377-67a0f3d55ec6"], "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 (68001-317-00)", "package_ndc": "68001-317-00", "marketing_start_date": "20170131"}], "brand_name": "Nadolol", "product_id": "68001-317_1980a55f-434f-5c45-e063-6394a90a014e", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "68001-317", "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": "ANDA203455", "marketing_category": "ANDA", "marketing_start_date": "20160223", "listing_expiration_date": "20261231"}