nadolol
Generic: nadolol
Labeler: american health packagingDrug Facts
Product Profile
Brand Name
nadolol
Generic Name
nadolol
Labeler
american health packaging
Dosage Form
TABLET
Routes
Active Ingredients
nadolol 40 mg/1
Manufacturer
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)
Mechanism of Action
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
60687898
Hyphenated Format
60687-898
Supplemental Identifiers
RxCUI
UNII
NUI
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
source: ndc
Resolved Composition
Strengths
- 40 mg/1
Packaging
- 30 BLISTER PACK in 1 CARTON (60687-898-21) / 1 TABLET in 1 BLISTER PACK (60687-898-11)
Packages (1)
Ingredients (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"}