Prescription drug · ANDA
Cartia XT (Diltiazem hydrochloride) NDC 72189-344
Diltiazem hydrochloride 300 mg/1 · Capsule, Extended release · Oral · DirectRx
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 72189-344-90 | 7218903449072189034490 | 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (72189-344-90)Marketed from Apr 6, 2022 |
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)
- Cartia XT
- Generic name (nonproprietary)
- diltiazem hydrochloride
- Active ingredients
- Diltiazem hydrochloride — 300 mg/1
- Dosage form
- Capsule, Extended release
- Route
- Oral
- Labeler
- DirectRxNDC labeler code 72189
- 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 72189-344_2c4c7b35-cdc7-a9c1-e063-6394a90a7634SPL ID 2c4c7b35-cdc7-a9c1-e063-6394a90a7634SPL set ID dbfda3a5-5602-6e47-e053-2995a90ac07bUNII 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
N472189034490followed by a unit qualifier and the quantityPackage 72189-0344-90. 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 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 72189-344
- What is NDC 72189-344?
- 72189-344 is the product NDC for Cartia XT (diltiazem hydrochloride), Diltiazem hydrochloride 300 mg/1 capsule, extended release, listed with the FDA by DirectRx. It has 1 package NDC, 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?
- DirectRx, NDC labeler code 72189. 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 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 |
| Cartia XTdiltiazem hydrochloride | Diltiazem hydrochloride 180 mg/1 | Capsule, Extended releaseOral | Bryant Ranch Prepack | 71335-0879 | 71335-0879-0171335-0879-02 |
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 180 mg/1 | Capsule, Extended releaseOral | Bryant Ranch Prepack | 71335-0879 |