What is NDC 69367-421?

69367-421 is the product NDC for Pindolol, Pindolol 5 mg/1 tablet, listed with the FDA by Westminster Pharmaceuticals, LLC. It has 1 package NDC, shown above in 10- and 11-digit form.

Westminster Pharmaceuticals, LLC, NDC labeler code 69367. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Pindolol?

18 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Pindolol NDC 69367-421 | National Drug Code

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	6936704210169367042101	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, LLCNDC labeler code 69367
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 205415
Marketing start: Nov 18, 2025
Listing expires: Dec 31, 2027
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

Current FDA label (SPL), effective Nov 25, 2025.

Indications (excerpt from the label)

INDICATIONS AND USAGE Pindolol tablets are indicated in the management of hypertension. It may be used alone or concomitantly with other antihypertensive agents, particularly with a thiazide-type diuretic.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 69367-421

What is NDC 69367-421?: 69367-421 is the product NDC for Pindolol, Pindolol 5 mg/1 tablet, listed with the FDA by Westminster Pharmaceuticals, LLC. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Pindolol.
What is the active ingredient?: Pindolol.
Who is the labeler?: Westminster Pharmaceuticals, LLC, NDC labeler code 69367. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Pindolol?: 18 other product NDCs are listed under this name. See all Pindolol NDCs.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other Pindolol NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Pindolol	Pindolol 10 mg/1	TabletOral	Westminster Pharmaceuticals, LLC	69367-422	69367-0422-01
Pindolol	Pindolol 5 mg/1	TabletOral	Bryant Ranch Prepack	72162-2652	72162-2652-01
Pindolol	Pindolol 10 mg/1	TabletOral	Bryant Ranch Prepack	72162-2653	72162-2653-01
Pindolol	Pindolol 5 mg/1	TabletOral	Proficient Rx LP	82804-939	82804-0939-0082804-0939-3082804-0939-55+4 more
Pindolol	Pindolol 10 mg/1	TabletOral	Proficient Rx LP	82804-940	82804-0940-0082804-0940-3082804-0940-55+4 more
Pindolol	Pindolol 5 mg/1	TabletOral	Marlex Pharmaceuticals, Inc.	10135-743	10135-0743-01
Pindolol	Pindolol 10 mg/1	TabletOral	Marlex Pharmaceuticals, Inc.	10135-744	10135-0744-01
Pindolol	Pindolol 5 mg/1	TabletOral	Bryant Ranch Prepack	63629-4828	63629-4828-01
Pindolol	Pindolol 10 mg/1	TabletOral	PD-Rx Pharmaceuticals, Inc.	72789-099	72789-0099-01
Pindolol	Pindolol 5 mg/1	TabletOral	PD-Rx Pharmaceuticals, Inc.	72789-100	72789-0100-01

All 19 Pindolol NDCs

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	Bryant Ranch Prepack	72162-2653
Pindolol	Pindolol 5 mg/1	TabletOral	Bryant Ranch Prepack	72162-2652
Pindolol	Pindolol 10 mg/1	TabletOral	Westminster Pharmaceuticals, LLC	69367-422
Pindolol	Pindolol 5 mg/1	TabletOral	Proficient Rx LP	82804-939
Pindolol	Pindolol 10 mg/1	TabletOral	Proficient Rx LP	82804-940