nadolol

Generic: nadolol

Labeler: american health packaging
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name nadolol
Generic Name nadolol
Labeler american health packaging
Dosage Form TABLET
Routes
ORAL
Active Ingredients

nadolol 40 mg/1

Manufacturer
American Health Packaging

Identifiers & Regulatory

Product NDC 60687-898
Product ID 60687-898_40d197a4-871c-104b-e063-6394a90a69fe
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA210955
Listing Expiration 2026-12-31
Marketing Start 2025-10-08

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 60687898
Hyphenated Format 60687-898

Supplemental Identifiers

RxCUI
198006 198007
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
  • 40 mg/1
source: ndc
Packaging
  • 30 BLISTER PACK in 1 CARTON (60687-898-21) / 1 TABLET in 1 BLISTER PACK (60687-898-11)
source: ndc

Packages (1)

Ingredients (1)

nadolol (40 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "40d197a4-871c-104b-e063-6394a90a69fe", "openfda": {"nui": ["N0000000161", "N0000175556"], "unii": ["FEN504330V"], "rxcui": ["198006", "198007"], "spl_set_id": ["9acc0c81-4145-43cc-b31a-7b1e3313259d"], "pharm_class_epc": ["beta-Adrenergic Blocker [EPC]"], "pharm_class_moa": ["Adrenergic beta-Antagonists [MoA]"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "30 BLISTER PACK in 1 CARTON (60687-898-21)  / 1 TABLET in 1 BLISTER PACK (60687-898-11)", "package_ndc": "60687-898-21", "marketing_start_date": "20251008"}], "brand_name": "Nadolol", "product_id": "60687-898_40d197a4-871c-104b-e063-6394a90a69fe", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "60687-898", "generic_name": "Nadolol", "labeler_name": "American Health Packaging", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Nadolol", "active_ingredients": [{"name": "NADOLOL", "strength": "40 mg/1"}], "application_number": "ANDA210955", "marketing_category": "ANDA", "marketing_start_date": "20251008", "listing_expiration_date": "20261231"}