Prescription drug · NDA AUTHORIZED GENERIC

Diltiazem Hydrochloride NDC 68682-708

diltiazem hydrochloride extended-release tablets · Diltiazem hydrochloride 360 mg/1 · Tablet, Extended release · Oral · Oceanside Pharmaceuticals

NDC codes

FDA NDC Directory
Product NDC (as listed)68682-708Labeler and product segments. Claims need a package NDC.
Product NDC at billing width68682-0708Add 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 NDC11-digit (billing)PackageCopy
68682-708-306868207083030 TABLET, EXTENDED RELEASE in 1 BOTTLE (68682-708-30)Marketed from Feb 6, 2014
68682-708-906868207089090 TABLET, EXTENDED RELEASE in 1 BOTTLE (68682-708-90)Marketed from Feb 6, 2014

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 extended-release tablets
Active ingredients
Diltiazem hydrochloride — 360 mg/1
Dosage form
Tablet, Extended release
Route
Oral
Product type
Prescription drug
Marketing category
NDA authorized genericApplication NDA 021392
Marketing start
Listing expires
Other FDA classes
Calcium Channel Antagonists (Mechanism)Cytochrome P450 3A4 Inhibitors (Mechanism)
Identifiers
Product ID 68682-708_9c3468f2-1199-4180-9e57-089b5353251aSPL ID 9c3468f2-1199-4180-9e57-089b5353251aSPL set ID 73b3607a-99d0-44d8-92ef-0074684c9d7dRxCUI 830874, 830877, 830879, 830882, 830897, 830900UNII 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

N468682070830 followed by a unit qualifier and the quantity

Package 68682-0708-30. 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 .

Indications (excerpt from the label)

Diltiazem Hydrochloride Extended-Release Tablets is a nondihydropyridine calcium channel blocker indicated for: • treatment of hypertension, to lower blood pressure. Lowering blood pressure reduces the risk of fatal and nonfatal cardiovascular events, primarily strokes and myocardial infarctions. It can be used alone or in combination with other antihypertensives. ( 1.1 ) • improving exercise tolerance in patients with chronic stable angina. ( 1.2 ) 1.1 Hypertension Diltiazem Hydrochloride Extended-Release Tablets are indicated for the treatment of hypertension, to lower blood pressure. Lowering blood pressure reduces the risk of fatal and nonfatal cardiovascular events, primarily strokes an…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under NDA 021392

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

FDA NDC Directory listings under NDA 021392
ProductStrengthForm · routeLabelerProduct NDC
Cardizem LAdiltiazem hydrochlorideDiltiazem hydrochloride 120 mg/1Tablet, Extended releaseOralBausch Health US LLC0187-2045
Cardizem LAdiltiazem hydrochlorideDiltiazem hydrochloride 180 mg/1Tablet, Extended releaseOralBausch Health US LLC0187-2046
Cardizem LAdiltiazem hydrochlorideDiltiazem hydrochloride 240 mg/1Tablet, Extended releaseOralBausch Health US LLC0187-2047
Cardizem LAdiltiazem hydrochlorideDiltiazem hydrochloride 300 mg/1Tablet, Extended releaseOralBausch Health US LLC0187-2048
Diltiazem Hydrochloridediltiazem hydrochloride extended-release tabletsDiltiazem hydrochloride 120 mg/1Tablet, Extended releaseOralOceanside Pharmaceuticals68682-704
Diltiazem Hydrochloridediltiazem hydrochloride extended-release tabletsDiltiazem hydrochloride 180 mg/1Tablet, Extended releaseOralOceanside Pharmaceuticals68682-705
Diltiazem Hydrochloridediltiazem hydrochloride extended-release tabletsDiltiazem hydrochloride 240 mg/1Tablet, Extended releaseOralOceanside Pharmaceuticals68682-706
Diltiazem Hydrochloridediltiazem hydrochloride extended-release tabletsDiltiazem hydrochloride 300 mg/1Tablet, Extended releaseOralOceanside Pharmaceuticals68682-707
Diltiazem Hydrochloridediltiazem hydrochloride extended-release tabletsDiltiazem hydrochloride 420 mg/1Tablet, Extended releaseOralOceanside Pharmaceuticals68682-709
Cardizem LAdiltiazem hydrochlorideDiltiazem hydrochloride 360 mg/1Tablet, Extended releaseOralBausch Health US LLC0187-2049
Cardizem LAdiltiazem hydrochlorideDiltiazem hydrochloride 420 mg/1Tablet, Extended releaseOralBausch Health US LLC0187-2050

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Diltiazem Hydrochloride NDC 68682-708 | Med-Code