What is NDC 82868-024?

82868-024 is the product NDC for Diltiazem Hydrochloride, Diltiazem hydrochloride 60 mg/1 tablet, 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 82868. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Diltiazem Hydrochloride?

220 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Diltiazem Hydrochloride NDC 82868-024 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)82868-024Labeler and product segments. Claims need a package NDC.

Product NDC at billing width82868-0024Add 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
82868-024-30	82868002430	30 TABLET in 1 BOTTLE, PLASTIC (82868-024-30)Marketed from Nov 3, 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): Diltiazem Hydrochloride
Generic name (nonproprietary): diltiazem hydrochloride
Active ingredients: Diltiazem hydrochloride — 60 mg/1
Dosage form: Tablet
Route: Oral
Labeler: Northwind Health Company, LLCNDC labeler code 82868
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 216521
Marketing start: Nov 3, 2023
Listing expires: Dec 31, 2027
Other FDA classes: Calcium Channel Antagonists (Mechanism)Cytochrome P450 3A4 Inhibitors (Mechanism)
Identifiers: Product ID 82868-024_47fc4881-8e2e-0e98-e063-6294a90af6d2SPL ID 47fc4881-8e2e-0e98-e063-6294a90af6d2SPL set ID 09a5d332-347b-e73d-e063-6294a90a67edRxCUI 831103UNII OLH94387TE
Pharmacologic class: Calcium Channel 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

N482868002430 followed by a unit qualifier and the quantity

Package 82868-0024-30. 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 Diltiazem hydrochloride tablets are indicated for the management of chronic stable angina and angina due to coronary artery spasm.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 82868-024

What is NDC 82868-024?: 82868-024 is the product NDC for Diltiazem Hydrochloride, Diltiazem hydrochloride 60 mg/1 tablet, 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?: Diltiazem Hydrochloride.
What is the active ingredient?: Diltiazem hydrochloride.
Who is the labeler?: Northwind Health Company, LLC, NDC labeler code 82868. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Diltiazem Hydrochloride?: 220 other product NDCs are listed under this name. See all Diltiazem 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 Diltiazem Hydrochloride NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Diltiazem hydrochloride	Diltiazem hydrochloride 30 mg/1	TabletOral	Viona Pharmaceuticals Inc	72578-199	72578-0199-0172578-0199-05
Diltiazem hydrochloride	Diltiazem hydrochloride 60 mg/1	TabletOral	Viona Pharmaceuticals Inc	72578-200	72578-0200-0172578-0200-05
Diltiazem hydrochloride	Diltiazem hydrochloride 90 mg/1	TabletOral	Viona Pharmaceuticals Inc	72578-201	72578-0201-0172578-0201-05
Diltiazem hydrochloride	Diltiazem hydrochloride 120 mg/1	TabletOral	Viona Pharmaceuticals Inc	72578-202	72578-0202-0172578-0202-05
Diltiazem hydrochloride	Diltiazem hydrochloride 60 mg/1	TabletOral	Zydus Lifesciences Limited	70771-1930	70771-1930-0170771-1930-05
Diltiazem hydrochloride	Diltiazem hydrochloride 30 mg/1	TabletOral	Zydus Lifesciences Limited	70771-1929	70771-1929-0170771-1929-05
Diltiazem hydrochloride	Diltiazem hydrochloride 90 mg/1	TabletOral	Zydus Lifesciences Limited	70771-1931	70771-1931-0170771-1931-05
Diltiazem hydrochloride	Diltiazem hydrochloride 120 mg/1	TabletOral	Zydus Lifesciences Limited	70771-1932	70771-1932-0170771-1932-05
Diltiazem Hydrochloride	Diltiazem hydrochloride 60 mg/1	Capsule, Extended releaseOral	Safecor Health LLC	48433-030	48433-0030-20
Diltiazem Hydrochloride	Diltiazem hydrochloride 90 mg/1	Capsule, Extended releaseOral	Safecor Health LLC	48433-031	48433-0031-20

All 221 Diltiazem Hydrochloride NDCs

Other NDCs under ANDA 216521

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

FDA NDC Directory listings under ANDA 216521
Product	Strength	Form · route	Labeler	Product NDC
Diltiazem Hydrochloride	Diltiazem hydrochloride 120 mg/1	TabletOral	Coupler LLC	67046-1560
Diltiazem Hydrochloride	Diltiazem hydrochloride 120 mg/1	TabletOral	ScieGen Pharmaceuticals, Inc	50228-484
Diltiazem Hydrochloride	Diltiazem hydrochloride 30 mg/1	TabletOral	ScieGen Pharmaceuticals, Inc	50228-481
Diltiazem Hydrochloride	Diltiazem hydrochloride 60 mg/1	TabletOral	ScieGen Pharmaceuticals, Inc	50228-482
Diltiazem Hydrochloride	Diltiazem hydrochloride 90 mg/1	TabletOral	ScieGen Pharmaceuticals, Inc	50228-483
Diltiazem Hydrochloride	Diltiazem hydrochloride 30 mg/1	TabletOral	Bryant Ranch Prepack	71335-2373
Diltiazem Hydrochloride	Diltiazem hydrochloride 30 mg/1	TabletOral	Coupler LLC	67046-1492
Diltiazem Hydrochloride	Diltiazem hydrochloride 90 mg/1	TabletOral	Bryant Ranch Prepack	71335-3135
Diltiazem Hydrochloride	Diltiazem hydrochloride 30 mg/1	TabletOral	Northwind Health Company, LLC	82868-036
Diltiazem Hydrochloride	Diltiazem hydrochloride 60 mg/1	TabletOral	A-S Medication Solutions	50090-7401