What is NDC 51655-322?

51655-322 is the product NDC for Labetalol Hydrochloride, Labetalol hydrochloride 100 mg/1 tablet, film coated, listed with the FDA by Northwind Health Company, LLC. It has 1 package NDC, shown above in 10- and 11-digit form.

Northwind Health Company, LLC, NDC labeler code 51655. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Labetalol Hydrochloride?

137 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Labetalol Hydrochloride NDC 51655-322

NDC codes

FDA NDC Directory

Product NDC (as listed)51655-322Labeler and product segments. Claims need a package NDC.

Product NDC at billing width51655-0322Add 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
51655-322-25	5165503222551655032225	60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-322-25)Marketed from Apr 25, 2023

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): Labetalol Hydrochloride
Generic name (nonproprietary): labetalol hydrochloride
Active ingredients: Labetalol hydrochloride — 100 mg/1
Dosage form: Tablet, Film coated
Route: Oral
Labeler: Northwind Health Company, LLCNDC labeler code 51655
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 209603
Marketing start: Apr 25, 2023
Listing expires: Dec 31, 2027
Other FDA classes: Adrenergic beta-Antagonists (Mechanism)
Identifiers: Product ID 51655-322_4b07a2c9-f7e6-9ea5-e063-6294a90a3e23SPL ID 4b07a2c9-f7e6-9ea5-e063-6294a90a3e23SPL set ID faf7a1ff-f18a-8ca7-e053-6394a90a1b1fRxCUI 896758UNII 1GEV3BAW9J
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

N451655032225 followed by a unit qualifier and the quantity

Package 51655-0322-25. 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 Jan 1, 2026.

Indications (excerpt from the label)

INDICATIONS AND USAGE Labetalol HCl tablets are indicated in the management of hypertension. Labetalol HCl tablets may be used alone or in combination with other antihypertensive agents, especially thiazide and loop diuretics.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 51655-322

What is NDC 51655-322?: 51655-322 is the product NDC for Labetalol Hydrochloride, Labetalol hydrochloride 100 mg/1 tablet, film coated, listed with the FDA by Northwind Health Company, LLC. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Labetalol Hydrochloride.
What is the active ingredient?: Labetalol hydrochloride.
Who is the labeler?: Northwind Health Company, LLC, NDC labeler code 51655. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Labetalol Hydrochloride?: 137 other product NDCs are listed under this name. See all Labetalol Hydrochloride 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 Labetalol Hydrochloride NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Labetalol Hydrochloride	Labetalol hydrochloride 200 mg/1	TabletOral	Coupler LLC	67046-1697	67046-1697-03
Labetalol Hydrochloride	Labetalol hydrochloride 100 mg/20mL	Injection, SolutionIntravenous	Armas Pharmaceuticals Inc.	72485-515	72485-0515-01
Labetalol Hydrochloride	Labetalol hydrochloride 100 mg/1	TabletOral	Coupler LLC	67046-1693	67046-1693-03
Labetalol Hydrochloride	Labetalol hydrochloride 300 mg/1	TabletOral	BluePoint Laboratories	68001-702	68001-0702-0068001-0702-03
Labetalol Hydrochloride	Labetalol hydrochloride 400 mg/1	TabletOral	Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.	23155-726	23155-0726-0123155-0726-05
Labetalol Hydrochloride	Labetalol hydrochloride 200 mg/1	TabletOral	NorthStar Rx LLC	72603-903	72603-0903-0172603-0903-02
Labetalol Hydrochloride	Labetalol hydrochloride 100 mg/1	TabletOral	NorthStar Rx LLC	72603-902	72603-0902-0172603-0902-02
Labetalol Hydrochloride	Labetalol hydrochloride 300 mg/1	TabletOral	NorthStar Rx LLC	72603-904	72603-0904-0172603-0904-02
Labetalol Hydrochloride	Labetalol hydrochloride 100 mg/1	TabletOral	BluePoint Laboratories	68001-700	68001-0700-0068001-0700-03
Labetalol Hydrochloride	Labetalol hydrochloride 200 mg/1	TabletOral	BluePoint Laboratories	68001-701	68001-0701-0068001-0701-03

All 138 Labetalol Hydrochloride NDCs

Other NDCs under ANDA 209603

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

FDA NDC Directory listings under ANDA 209603
Product	Strength	Form · route	Labeler	Product NDC
Labetalol Hydrochloride	Labetalol hydrochloride 300 mg/1	Tablet, Film coatedOral	RedPharm Drug	67296-2114
Labetalol Hydrochloride	Labetalol hydrochloride 100 mg/1	Tablet, Film coatedOral	Proficient Rx LP	82804-289
Labetalol Hydrochloride	Labetalol hydrochloride 100 mg/1	Tablet, Film coatedOral	Major Pharmaceuticals	0904-7451
Labetalol Hydrochloride	Labetalol hydrochloride 200 mg/1	Tablet, Film coatedOral	Major Pharmaceuticals	0904-7452
Labetalol Hydrochloride	Labetalol hydrochloride 300 mg/1	Tablet, Film coatedOral	Major Pharmaceuticals	0904-7453
Labetalol Hydrochloride	Labetalol hydrochloride 200 mg/1	Tablet, Film coatedOral	Golden State Medical Supply, Inc.	51407-615
Labetalol Hydrochloride	Labetalol hydrochloride 100 mg/1	Tablet, Film coatedOral	Golden State Medical Supply, Inc.	51407-614
Labetalol Hydrochloride	Labetalol hydrochloride 200 mg/1	Tablet, Film coatedOral	NuCare Pharmaceuticals , Inc.	68071-3878
Labetalol Hydrochloride	Labetalol hydrochloride 300 mg/1	Tablet, Film coatedOral	Golden State Medical Supply, Inc.	51407-616
Labetalol Hydrochloride	Labetalol hydrochloride 100 mg/1	Tablet, Film coatedOral	A-S Medication Solutions	50090-7458
Labetalol Hydrochloride	Labetalol hydrochloride 100 mg/1	Tablet, Film coatedOral	A-S Medication Solutions	50090-7457
Labetalol Hydrochloride	Labetalol hydrochloride 100 mg/1	Tablet, Film coatedOral	Biocon Pharma Inc.	70377-060
Labetalol Hydrochloride	Labetalol hydrochloride 200 mg/1	Tablet, Film coatedOral	Biocon Pharma Inc.	70377-061
Labetalol Hydrochloride	Labetalol hydrochloride 300 mg/1	Tablet, Film coatedOral	Biocon Pharma Inc.	70377-062
Labetalol Hydrochloride	Labetalol hydrochloride 400 mg/1	Tablet, Film coatedOral	Biocon Pharma Inc.	70377-063
Labetalol Hydrochloride	Labetalol hydrochloride 100 mg/1	Tablet, Film coatedOral	NCS HealthCare of KY, LLC dba Vangard Labs	0615-8512
Labetalol Hydrochloride	Labetalol hydrochloride 300 mg/1	Tablet, Film coatedOral	A-S Medication Solutions	50090-7743
Labetalol Hydrochloride	Labetalol hydrochloride 200 mg/1	Tablet, Film coatedOral	NCS HealthCare of KY, LLC dba Vangard Labs	0615-8513
Labetalol Hydrochloride	Labetalol hydrochloride 200 mg/1	Tablet, Film coatedOral	A-S Medication Solutions	50090-7524
Labetalol Hydrochloride	Labetalol hydrochloride 200 mg/1	Tablet, Film coatedOral	A-S Medication Solutions	50090-7523

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