What is NDC 68682-008?

68682-008 is the product NDC for Diltiazem Hydrochloride, Diltiazem hydrochloride 90 mg/1 tablet, listed with the FDA by Oceanside Pharmaceuticals. It has 2 package NDCs, shown above in 10- and 11-digit form.

Oceanside Pharmaceuticals, NDC labeler code 68682. 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?

223 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 68682-008

NDC codes

FDA NDC Directory

Product NDC (as listed)68682-008Labeler and product segments. Claims need a package NDC.

Product NDC at billing width68682-0008Add 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
68682-008-10	6868200081068682000810	100 TABLET in 1 BOTTLE (68682-008-10)Marketed from Dec 25, 2010
68682-008-50	6868200085068682000850	500 TABLET in 1 BOTTLE (68682-008-50)Marketed from Dec 25, 2010

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 — 90 mg/1
Dosage form: Tablet
Route: Oral
Labeler: Oceanside PharmaceuticalsNDC labeler code 68682
Product type: Prescription drug
Marketing category: NDA authorized genericApplication NDA 018602
Marketing start: Dec 25, 2010
Listing expires: Dec 31, 2027
Other FDA classes: Calcium Channel Antagonists (Mechanism)
Identifiers: Product ID 68682-008_06626a5d-987f-4d1c-9ffc-28fd51362900SPL ID 06626a5d-987f-4d1c-9ffc-28fd51362900SPL set ID f6a24de7-8ffe-48af-873f-10fdcd5551d1RxCUI 831054, 831102, 831103, 833217UNII OLH94387TEUPC 0368682006100, 0368682009101, 0368682008104, 0368682007107
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

N468682000810 followed by a unit qualifier and the quantity

Package 68682-0008-10. 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 Jun 2, 2020.

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 68682-008

What is NDC 68682-008?: 68682-008 is the product NDC for Diltiazem Hydrochloride, Diltiazem hydrochloride 90 mg/1 tablet, listed with the FDA by Oceanside Pharmaceuticals. It has 2 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?: Oceanside Pharmaceuticals, NDC labeler code 68682. 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?: 223 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 60 mg/1	Capsule, Extended releaseOral	Cranbury Pharmaceuticals, LLC	27808-322	27808-0322-01
Diltiazem Hydrochloride	Diltiazem hydrochloride 90 mg/1	Capsule, Extended releaseOral	Cranbury Pharmaceuticals, LLC	27808-323	27808-0323-01
Diltiazem Hydrochloride	Diltiazem hydrochloride 120 mg/1	Capsule, Extended releaseOral	Cranbury Pharmaceuticals, LLC	27808-324	27808-0324-01
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

All 224 Diltiazem Hydrochloride NDCs

Other NDCs under NDA 018602

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

FDA NDC Directory listings under NDA 018602
Product	Strength	Form · route	Labeler	Product NDC
Cardizemdiltiazem hydrochloride	Diltiazem hydrochloride 30 mg/1	Tablet, CoatedOral	Bausch Health US LLC	0187-0771
Cardizemdiltiazem hydrochloride	Diltiazem hydrochloride 60 mg/1	Tablet, CoatedOral	Bausch Health US LLC	0187-0772
Cardizemdiltiazem hydrochloride	Diltiazem hydrochloride 120 mg/1	Tablet, CoatedOral	Bausch Health US LLC	0187-0792
Diltiazem Hydrochloride	Diltiazem hydrochloride 120 mg/1	TabletOral	NuCare Pharmaceuticals,Inc.	68071-4242
Diltiazem Hydrochloride	Diltiazem hydrochloride 30 mg/1	TabletOral	Oceanside Pharmaceuticals	68682-006
Diltiazem Hydrochloride	Diltiazem hydrochloride 60 mg/1	TabletOral	Oceanside Pharmaceuticals	68682-007
Diltiazem Hydrochloride	Diltiazem hydrochloride 120 mg/1	TabletOral	Oceanside Pharmaceuticals	68682-009
Diltiazem Hydrochloride	Diltiazem hydrochloride 90 mg/1	TabletOral	Bryant Ranch Prepack	71335-0579