Prescription drug · ANDA
Diltiazem Hydrochloride NDC 62135-335
Diltiazem hydrochloride 90 mg/1 · Tablet · Oral · Chartwell RX, LLC
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 62135-335-90 | 62135033590 | 90 TABLET in 1 BOTTLE (62135-335-90)Marketed from Jun 17, 2024 |
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 — 90 mg/1
- Dosage form
- Tablet
- Route
- Oral
- Labeler
- Chartwell RX, LLC
- Product type
- Prescription drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 074093
- Marketing start
- Listing expires
- Other FDA classes
- Calcium Channel Antagonists (Mechanism)Cytochrome P450 3A4 Inhibitors (Mechanism)
- Identifiers
- Product ID 62135-335_1b432d9d-b46c-2ee8-e063-6294a90adb54SPL ID 1b432d9d-b46c-2ee8-e063-6294a90adb54SPL set ID 51abce7b-e3d1-44b5-bccc-d463150d0bbaRxCUI 831054, 831102, 831103, 833217UNII OLH94387TEUPC 0362135334123, 0362135336905, 0362135335908, 0362135333126
- 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
N462135033590followed by a unit qualifier and the quantityPackage 62135-0335-90. 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)
INDICATIONS AND USAGE Diltiazem hydrochloride is indicated for the management of chronic stable angina and angina due to coronary artery spasm.
Excerpt only. Read the full label for complete information.
Other NDCs under ANDA 074093
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 |
|---|---|---|---|---|
| Diltiazem Hydrochloride | Diltiazem hydrochloride 120 mg/1 | TabletOral | Chartwell RX, LLC | 62135-336 |
| Diltiazem Hydrochloride | Diltiazem hydrochloride 30 mg/1 | TabletOral | Chartwell RX, LLC | 62135-333 |
| Diltiazem Hydrochloride | Diltiazem hydrochloride 60 mg/1 | TabletOral | Chartwell RX, LLC | 62135-334 |