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 20 mg/1

Manufacturer
American Health Packaging

Identifiers & Regulatory

Product NDC 60687-302
Product ID 60687-302_3a9ec2d2-d927-064b-e063-6294a90a1226
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA203455
Listing Expiration 2026-12-31
Marketing Start 2017-05-22

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 60687302
Hyphenated Format 60687-302

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 ANDA203455 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • HOW SUPPLIED Nadolol Tablets, USP are supplied as: 20 mg tablets : Yellow, round, biconvex tablets debossed "347" on one side and 'I' on the left side of the bisect and 'G' on the right side of bisect on other. Unit dose packages of 30 (5 x 6) NDC 60687-302-25 40 mg tablets: Yellow, round, biconvex tablets debossed "348" on one side and 'I' on the left side of the bisect and 'G' on the right side of bisect on other. Unit dose packages of 30 (5 x 6) NDC 60687-313-25 STORAGE Store at 20° to 25°C (68° to 77°F). [See USP Controlled Room Temperature.] Protect from light. FOR YOUR PROTECTION: Do not use if blister is torn or broken.
  • Package/Label Display Panel – Carton – 20 mg NDC 60687- 302 -25 Nadolol Tablets, USP 20 mg 30 Tablets (5 x 6) Rx Only Each Tablet Contains: Nadolol, USP................................................................20 mg Usual Dosage: See full prescribing information. Store at 20° to 25°C (68° to 77°F); excursions permitted between 15° to 30°C (59° to 86°F) [see USP Controlled Room Temperature]. Protect from light. FOR YOUR PROTECTION: Do not use if blister is torn or broken. The drug product contained in this package is from NDC # 68001-317, BluePoint Laboratories. Distributed by: American Health Packaging, Columbus, Ohio 43217 730225 0430225/0124 20 mg Nadolol Tablets Carton
  • Package/Label Display Panel – Blister – 20 mg Nadolol Tablet, USP 20 mg 20 mg Nadolol Tablet Blister
  • Package/Label Display Panel – Carton – 40 mg NDC 60687- 313 -25 Nadolol Tablets, USP 40 mg 30 Tablets (5 x 6) Rx Only Each Tablet Contains: Nadolol, USP................................................................40 mg Usual Dosage: See full prescribing information. Store at 20° to 25°C (68° to 77°F); excursions permitted between 15° to 30°C (59° to 86°F) [see USP Controlled Room Temperature]. Protect from light. FOR YOUR PROTECTION: Do not use if blister is torn or broken. The drug product contained in this package is from NDC # 68001-318, BluePoint Laboratories. Distributed by: American Health Packaging, Columbus, Ohio 43217 731325 0431325/0224 40 mg Nadolol Tablets Carton
  • Package/Label Display Panel – Blister – 40 mg Nadolol Tablet, USP 40 mg 40 mg Nadolol Tablet Blister
source: label

Packages (0)

No package records.

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": "3a9ec2d2-d927-064b-e063-6294a90a1226", "openfda": {"nui": ["N0000000161", "N0000175556"], "unii": ["FEN504330V"], "rxcui": ["198006", "198007"], "spl_set_id": ["9e8e129d-cb17-45fc-b3e2-2600c0166463"], "pharm_class_epc": ["beta-Adrenergic Blocker [EPC]"], "pharm_class_moa": ["Adrenergic beta-Antagonists [MoA]"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [], "brand_name": "Nadolol", "product_id": "60687-302_3a9ec2d2-d927-064b-e063-6294a90a1226", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "60687-302", "generic_name": "Nadolol", "labeler_name": "American Health Packaging", "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": "20170522", "listing_expiration_date": "20261231"}