Prescription drug · ANDA
Cartia XT (Diltiazem hydrochloride) NDC 71335-0879
Diltiazem hydrochloride 180 mg/1 · Capsule, Extended release · Oral · Bryant Ranch Prepack
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 71335-0879-1 | 7133508790171335087901 | 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71335-0879-1)Marketed from Jun 25, 2018 | |
| 71335-0879-2 | 7133508790271335087902 | 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71335-0879-2)Marketed from Dec 27, 2021 |
How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 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)
- Cartia XTSuffix: XT
- Generic name (nonproprietary)
- diltiazem hydrochloride
- Active ingredients
- Diltiazem hydrochloride — 180 mg/1
- Dosage form
- Capsule, Extended release
- Route
- Oral
- Labeler
- Bryant Ranch PrepackNDC labeler code 71335
- Product type
- Prescription drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 074752
- Marketing start
- Listing expires
- Other FDA classes
- Calcium Channel Antagonists (Mechanism)Cytochrome P450 3A4 Inhibitors (Mechanism)
- Identifiers
- Product ID 71335-0879_053455c6-3889-4a52-9981-db90a6bce8edSPL ID 053455c6-3889-4a52-9981-db90a6bce8edSPL set ID e02f5fad-6482-4d5d-91c5-0ae6b0ce15b8RxCUI 830845, 831255UNII 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
N471335087901followed by a unit qualifier and the quantityPackage 71335-0879-01. 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)
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.
About NDC 71335-0879
- What is NDC 71335-0879?
- 71335-0879 is the product NDC for Cartia XT (diltiazem hydrochloride), Diltiazem hydrochloride 180 mg/1 capsule, extended release, listed with the FDA by Bryant Ranch Prepack. It has 2 package NDCs, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- Cartia XT (Diltiazem Hydrochloride).
- What is the active ingredient?
- Diltiazem hydrochloride.
- Who is the labeler?
- Bryant Ranch Prepack, NDC labeler code 71335. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for Cartia XT?
- 6 other product NDCs are listed under this name. See all Cartia XT NDCs.
- Is there a related HCPCS / J-code?
- Not in Med-Code's curated HCPCS directory. See Billing references above.
Related NDCs: other Cartia XT products
Other finished products listed under the same name: strengths, forms and labelers.
| Product | Strength | Form · route | Labeler | Product NDC | Package NDCs (11-digit) |
|---|---|---|---|---|---|
| Cartia XTdiltiazem hydrochloride | Diltiazem hydrochloride 300 mg/1 | Capsule, Extended releaseOral | DirectRx | 72189-344 | 72189-0344-90 |
| Cartia XTdiltiazem hydrochloride | Diltiazem hydrochloride 120 mg/1 | Capsule, Extended releaseOral | Actavis Pharma, Inc. | 62037-597 | 62037-0597-0562037-0597-90 |
| Cartia XTdiltiazem hydrochloride | Diltiazem hydrochloride 180 mg/1 | Capsule, Extended releaseOral | Actavis Pharma, Inc. | 62037-598 | 62037-0598-0562037-0598-90 |
| Cartia XTdiltiazem hydrochloride | Diltiazem hydrochloride 240 mg/1 | Capsule, Extended releaseOral | Actavis Pharma, Inc. | 62037-599 | 62037-0599-0562037-0599-90 |
| Cartia XTdiltiazem hydrochloride | Diltiazem hydrochloride 300 mg/1 | Capsule, Extended releaseOral | Actavis Pharma, Inc. | 62037-600 | 62037-0600-0562037-0600-90 |
| Cartia XTdiltiazem hydrochloride | Diltiazem hydrochloride 120 mg/1 | Capsule, Extended releaseOral | Bryant Ranch Prepack | 63629-7896 | 63629-7896-0163629-7896-02 |
Other NDCs under ANDA 074752
Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.
| Product | Strength | Form · route | Labeler | Product NDC |
|---|---|---|---|---|
| Cartia XTdiltiazem hydrochloride | Diltiazem hydrochloride 120 mg/1 | Capsule, Extended releaseOral | Actavis Pharma, Inc. | 62037-597 |
| Cartia XTdiltiazem hydrochloride | Diltiazem hydrochloride 180 mg/1 | Capsule, Extended releaseOral | Actavis Pharma, Inc. | 62037-598 |
| Cartia XTdiltiazem hydrochloride | Diltiazem hydrochloride 240 mg/1 | Capsule, Extended releaseOral | Actavis Pharma, Inc. | 62037-599 |
| Cartia XTdiltiazem hydrochloride | Diltiazem hydrochloride 300 mg/1 | Capsule, Extended releaseOral | Actavis Pharma, Inc. | 62037-600 |
| Cartia XTdiltiazem hydrochloride | Diltiazem hydrochloride 120 mg/1 | Capsule, Extended releaseOral | Bryant Ranch Prepack | 63629-7896 |
| Cartia XTdiltiazem hydrochloride | Diltiazem hydrochloride 300 mg/1 | Capsule, Extended releaseOral | DirectRx | 72189-344 |