Pindolol NDC 69367-421

NDC codes

FDA NDC Directory

Product NDC (as listed)69367-421Labeler and product segments. Claims need a package NDC.

Product NDC at billing width69367-0421Add 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
69367-421-01	69367042101	100 TABLET in 1 BOTTLE (69367-421-01)Marketed from Nov 18, 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): Pindolol
Generic name (nonproprietary): pindolol
Active ingredients: Pindolol — 5 mg/1
Dosage form: Tablet
Route: Oral
Labeler: Westminster Pharmaceuticals, LLC
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 205415
Marketing start: Nov 18, 2025
Listing expires: Dec 31, 2026
Other FDA classes: Adrenergic beta-Antagonists (Mechanism)
Identifiers: Product ID 69367-421_cd3e9748-5b81-47f6-881c-648b3e2c4d3dSPL ID cd3e9748-5b81-47f6-881c-648b3e2c4d3dSPL set ID efdb0189-37b5-45d6-b92c-1157bb9df789RxCUI 198104, 198105UNII BJ4HF6IU1D
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

N469367042101 followed by a unit qualifier and the quantity

Package 69367-0421-01. 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 205415

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

FDA NDC Directory listings under ANDA 205415
Product	Strength	Form · route	Labeler	Product NDC
Pindolol	Pindolol 10 mg/1	TabletOral	Westminster Pharmaceuticals, LLC	69367-422
Pindolol	Pindolol 5 mg/1	TabletOral	Bryant Ranch Prepack	72162-2652
Pindolol	Pindolol 10 mg/1	TabletOral	Bryant Ranch Prepack	72162-2653
Pindolol	Pindolol 10 mg/1	TabletOral	Proficient Rx LP	82804-940
Pindolol	Pindolol 5 mg/1	TabletOral	Proficient Rx LP	82804-939