NDC codes

FDA NDC Directory
Product NDC (as listed)51407-979Labeler and product segments. Claims need a package NDC.
Product NDC at billing width51407-0979Add 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 NDC11-digit (billing)PackageCopy
51407-979-0151407097901100 TABLET in 1 BOTTLE (51407-979-01)Marketed from Apr 1, 2025

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
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 210955
Marketing start
Listing expires
Other FDA classes
Adrenergic beta-Antagonists (Mechanism)
Identifiers
Product ID 51407-979_4b31bd46-93da-ed99-e063-6394a90a827fSPL ID 4b31bd46-93da-ed99-e063-6394a90a827fSPL set ID 33dcfdb9-1741-71e1-e063-6294a90afdffRxCUI 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

N451407097901 followed by a unit qualifier and the quantity

Package 51407-0979-01. 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 210955

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

FDA NDC Directory listings under ANDA 210955
ProductStrengthForm · routeLabelerProduct NDC
NadololNadolol 20 mg/1TabletOralGolden State Medical Supply, Inc.51407-977
NadololNadolol 80 mg/1TabletOralBryant Ranch Prepack72162-2198
NadololNadolol 40 mg/1TabletOralGolden State Medical Supply, Inc.51407-978
NadololNadolol 20 mg/1TabletOralUNICHEM PHARMACEUTICALS (USA), INC.76385-133
NadololNadolol 40 mg/1TabletOralUNICHEM PHARMACEUTICALS (USA), INC.76385-134
NadololNadolol 80 mg/1TabletOralUNICHEM PHARMACEUTICALS (USA), INC.76385-135
NadololNadolol 20 mg/1TabletOralAmerican Health Packaging60687-887
NadololNadolol 40 mg/1TabletOralAmerican Health Packaging60687-898
NadololNadolol 80 mg/1TabletOralBryant Ranch Prepack71335-2131
NadololNadolol 20 mg/1TabletOralBluePoint Laboratories68001-630
NadololNadolol 40 mg/1TabletOralBluePoint Laboratories68001-631
NadololNadolol 80 mg/1TabletOralBluePoint Laboratories68001-632

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