What is NDC 62332-817?

62332-817 is the product NDC for Diltiazem Hydrochloride, Diltiazem hydrochloride 240 mg/1 capsule, extended release, listed with the FDA by Alembic Pharmaceuticals Inc.. It has 3 package NDCs, shown above in 10- and 11-digit form.

Alembic Pharmaceuticals Inc., NDC labeler code 62332. 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 62332-817 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)62332-817Labeler and product segments. Claims need a package NDC.

Product NDC at billing width62332-0817Add 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
62332-817-31	62332081731	100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (62332-817-31)Marketed from Oct 28, 2024
62332-817-71	62332081771	500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (62332-817-71)Marketed from Oct 28, 2024
62332-817-91	62332081791	1000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (62332-817-91)Marketed from Oct 28, 2024

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 — 240 mg/1
Dosage form: Capsule, Extended release
Route: Oral
Labeler: Alembic Pharmaceuticals Inc.NDC labeler code 62332
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 218587
Marketing start: Oct 28, 2024
Listing expires: Dec 31, 2027
Other FDA classes: Calcium Channel Antagonists (Mechanism)Cytochrome P450 3A4 Inhibitors (Mechanism)
Identifiers: Product ID 62332-817_e01b87fe-c495-4a9f-8195-2b6728d738d4SPL ID e01b87fe-c495-4a9f-8195-2b6728d738d4SPL set ID 04a85be5-f746-418e-8e37-292703f16934RxCUI 830837, 830845, 830861UNII OLH94387TEUPC 0362332816316, 0362332815319
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

N462332081731 followed by a unit qualifier and the quantity

Package 62332-0817-31. 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 Apr 29, 2026.

Indications (excerpt from the label)

INDICATIONS AND USAGE Diltiazem hydrochloride extended-release capsules are indicated for the treatment of hypertension. Diltiazem hydrochloride may be used alone or in combination with other antihypertensive medications, such as diuretics. Diltiazem hydrochloride extended-release capsules are indicated for the management of chronic stable angina.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 62332-817

What is NDC 62332-817?: 62332-817 is the product NDC for Diltiazem Hydrochloride, Diltiazem hydrochloride 240 mg/1 capsule, extended release, listed with the FDA by Alembic Pharmaceuticals Inc.. It has 3 package NDCs, 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?: Alembic Pharmaceuticals Inc., NDC labeler code 62332. 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	Zydus Lifesciences Limited	70771-1929	70771-1929-0170771-1929-05
Diltiazem hydrochloride	Diltiazem hydrochloride 60 mg/1	TabletOral	Zydus Lifesciences Limited	70771-1930	70771-1930-0170771-1930-05
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 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	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 218587

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

FDA NDC Directory listings under ANDA 218587
Product	Strength	Form · route	Labeler	Product NDC
Diltiazem Hydrochloride	Diltiazem hydrochloride 120 mg/1	Capsule, Extended releaseOral	Alembic Pharmaceuticals Inc.	62332-815
Diltiazem Hydrochloride	Diltiazem hydrochloride 180 mg/1	Capsule, Extended releaseOral	Alembic Pharmaceuticals Inc.	62332-816
Diltiazem Hydrochloride	Diltiazem hydrochloride 180 mg/1	Capsule, Extended releaseOral	Alembic Pharmaceuticals Limited	46708-816
Diltiazem Hydrochloride	Diltiazem hydrochloride 120 mg/1	Capsule, Extended releaseOral	Alembic Pharmaceuticals Limited	46708-815
Diltiazem Hydrochloride	Diltiazem hydrochloride 240 mg/1	Capsule, Extended releaseOral	Alembic Pharmaceuticals Limited	46708-817