Prescription drug · ANDA
Diltiazem Hydrochloride NDC 71335-3135
Diltiazem hydrochloride 90 mg/1 · Tablet · Oral · Bryant Ranch Prepack
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 71335-3135-1 | 71335313501 | 30 TABLET in 1 BOTTLE (71335-3135-1)Marketed from May 27, 2026 | |
| 71335-3135-2 | 71335313502 | 90 TABLET in 1 BOTTLE (71335-3135-2)Marketed from May 27, 2026 |
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)
- Diltiazem Hydrochloride
- Generic name (nonproprietary)
- diltiazem hydrochloride
- Active ingredients
- Diltiazem hydrochloride — 90 mg/1
- Dosage form
- Tablet
- Route
- Oral
- Labeler
- Bryant Ranch Prepack
- Product type
- Prescription drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 216521
- Marketing start
- Listing expires
- Other FDA classes
- Calcium Channel Antagonists (Mechanism)Cytochrome P450 3A4 Inhibitors (Mechanism)
- Identifiers
- Product ID 71335-3135_381c8c9a-95ec-464b-a264-aae326e866c8SPL ID 381c8c9a-95ec-464b-a264-aae326e866c8SPL set ID 50df9f09-aa2f-495d-a25c-7c5c0fdffcf0RxCUI 831102UNII 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
N471335313501followed by a unit qualifier and the quantityPackage 71335-3135-01. 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 tablets 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.
Other NDCs under ANDA 216521
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 30 mg/1 | TabletOral | Coupler LLC | 67046-1492 |
| Diltiazem Hydrochloride | Diltiazem hydrochloride 30 mg/1 | TabletOral | Bryant Ranch Prepack | 71335-2373 |
| Diltiazem Hydrochloride | Diltiazem hydrochloride 60 mg/1 | TabletOral | Northwind Health Company, LLC | 82868-024 |
| Diltiazem Hydrochloride | Diltiazem hydrochloride 60 mg/1 | TabletOral | A-S Medication Solutions | 50090-7401 |
| Diltiazem Hydrochloride | Diltiazem hydrochloride 30 mg/1 | TabletOral | Northwind Health Company, LLC | 82868-036 |
| Diltiazem Hydrochloride | Diltiazem hydrochloride 120 mg/1 | TabletOral | Coupler LLC | 67046-1560 |
| Diltiazem Hydrochloride | Diltiazem hydrochloride 30 mg/1 | TabletOral | ScieGen Pharmaceuticals, Inc | 50228-481 |
| Diltiazem Hydrochloride | Diltiazem hydrochloride 60 mg/1 | TabletOral | ScieGen Pharmaceuticals, Inc | 50228-482 |
| Diltiazem Hydrochloride | Diltiazem hydrochloride 90 mg/1 | TabletOral | ScieGen Pharmaceuticals, Inc | 50228-483 |
| Diltiazem Hydrochloride | Diltiazem hydrochloride 120 mg/1 | TabletOral | ScieGen Pharmaceuticals, Inc | 50228-484 |