Diltiazem Hydrochloride NDC 47335-679

NDC codes

FDA NDC Directory

Product NDC (as listed)47335-679Labeler and product segments. Claims need a package NDC.

Product NDC at billing width47335-0679Add 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
47335-679-13	47335067913	500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (47335-679-13)Marketed from Oct 31, 2011
47335-679-18	47335067918	1000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (47335-679-18)Marketed from Oct 31, 2011
47335-679-19	47335067919	90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (47335-679-19)Marketed from Oct 31, 2011
47335-679-81	47335067981	90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (47335-679-81)Marketed from Oct 31, 2011
47335-679-83	47335067983	30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (47335-679-83)Marketed from Oct 31, 2011

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 — 360 mg/1
Dosage form: Capsule, Extended release
Route: Oral
Labeler: Sun Pharmaceutical Industries, Inc.
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 090492
Marketing start: Oct 31, 2011
Listing expires: Dec 31, 2026
Other FDA classes: Calcium Channel Antagonists (Mechanism)
Identifiers: Product ID 47335-679_3c94f868-93d3-4b36-8420-b2903a0bd79aSPL ID 3c94f868-93d3-4b36-8420-b2903a0bd79aSPL set ID 6f71ba5e-7bd6-409a-80c6-2f22d975aefcRxCUI 830795, 830801, 830837, 830845, 830861UNII OLH94387TEUPC 0347335679830, 0347335677836, 0347335676839, 0347335678833, 0347335675832
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

N447335067913 followed by a unit qualifier and the quantity

Package 47335-0679-13. 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 9, 2023.

Indications (excerpt from the label)

INDICATIONS AND USAGE Diltiazem hydrochloride extended-release capsules (Once-a-day dosage) are indicated for the treatment of hypertension. It may be used alone or in combination with other antihypertensive medications. Diltiazem hydrochloride extended-release capsules (Once-a-day dosage) 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)

Other NDCs under ANDA 090492

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

FDA NDC Directory listings under ANDA 090492
Product	Strength	Form · route	Labeler	Product NDC
Diltiazem Hydrochloride	Diltiazem hydrochloride 180 mg/1	Capsule, Extended releaseOral	Sun Pharmaceutical Industries, Inc.	47335-676
Diltiazem Hydrochloride	Diltiazem hydrochloride 120 mg/1	Capsule, Extended releaseOral	Sun Pharmaceutical Industries, Inc.	47335-675
Diltiazem Hydrochloride	Diltiazem hydrochloride 240 mg/1	Capsule, Extended releaseOral	Sun Pharmaceutical Industries, Inc.	47335-677
Diltiazem Hydrochloride	Diltiazem hydrochloride 300 mg/1	Capsule, Extended releaseOral	Sun Pharmaceutical Industries, Inc.	47335-678