Nadolol NDC 59651-252

NDC codes

FDA NDC Directory

Product NDC (as listed)59651-252Labeler and product segments. Claims need a package NDC.

Product NDC at billing width59651-0252Add the package segment from the table below.

Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC	11-digit (billing)	Package	Copy
59651-252-01	59651025201	100 TABLET in 1 BOTTLE (59651-252-01)Marketed from Oct 29, 2021

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules

Product information

Brand name (proprietary): Nadolol
Generic name (nonproprietary): nadolol
Active ingredients: Nadolol — 80 mg/1
Dosage form: Tablet
Route: Oral
Labeler: Aurobindo Pharma Limited
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 201893
Marketing start: Oct 29, 2021
Listing expires: Dec 31, 2026
Other FDA classes: Adrenergic beta-Antagonists (Mechanism)
Identifiers: Product ID 59651-252_bfed393e-1baf-439a-8073-998c1a97b276SPL ID bfed393e-1baf-439a-8073-998c1a97b276SPL set ID 44c5352d-89f8-4bd3-9479-1069304562caRxCUI 198006, 198007, 198008UNII FEN504330V
Pharmacologic class: beta-Adrenergic Blocker

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N459651025201 followed by a unit qualifier and the quantity

Package 59651-0252-01. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

Label details couldn’t be retrieved right now. Open the label on DailyMed.

Other NDCs under ANDA 201893

Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.

FDA NDC Directory listings under ANDA 201893
Product	Strength	Form · route	Labeler	Product NDC
Nadolol	Nadolol 40 mg/1	TabletOral	BluePoint Laboratories	68001-691
Nadolol	Nadolol 20 mg/1	TabletOral	BluePoint Laboratories	68001-690
Nadolol	Nadolol 80 mg/1	TabletOral	BluePoint Laboratories	68001-692
Nadolol	Nadolol 40 mg/1	TabletOral	Aurobindo Pharma Limited	59651-251
Nadolol	Nadolol 40 mg/1	TabletOral	REMEDYREPACK INC.	70518-4662
Nadolol	Nadolol 20 mg/1	TabletOral	Aurobindo Pharma Limited	59651-589