Prescription drug · ANDA
Cartia XT (Diltiazem hydrochloride) NDC 62037-599
Diltiazem hydrochloride 240 mg/1 · Capsule, Extended release · Oral · Actavis Pharma, Inc.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 62037-599-05 | 6203705990562037059905 | 500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (62037-599-05)Marketed from Jun 23, 1999 | |
| 62037-599-90 | 6203705999062037059990 | 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (62037-599-90)Marketed from Jun 23, 1999 |
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 XTSuffix: XT
- Generic name (nonproprietary)
- diltiazem hydrochloride
- Active ingredients
- Diltiazem hydrochloride — 240 mg/1
- Dosage form
- Capsule, Extended release
- Route
- Oral
- Labeler
- Actavis Pharma, Inc.NDC labeler code 62037
- 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 62037-599_03bf4273-4fcb-4248-94d0-7de48ce210f4SPL ID 03bf4273-4fcb-4248-94d0-7de48ce210f4
- 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
N462037059905followed by a unit qualifier and the quantityPackage 62037-0599-05. 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
The FDA listing for this product does not reference a label (SPL) set.
About NDC 62037-599
- What is NDC 62037-599?
- 62037-599 is the product NDC for Cartia XT (diltiazem hydrochloride), Diltiazem hydrochloride 240 mg/1 capsule, extended release, listed with the FDA by Actavis Pharma, Inc.. 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?
- Actavis Pharma, Inc., NDC labeler code 62037. 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 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 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 |
| Cartia XTdiltiazem hydrochloride | Diltiazem hydrochloride 300 mg/1 | Capsule, Extended releaseOral | DirectRx | 72189-344 |