diltiazem hydrochloride
- Product NDC
- 71335-2602
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- diltiazem hydrochloride
- Dosage form
- CAPSULE, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA208783
- Marketing category
- ANDA
- Substance
- DILTIAZEM HYDROCHLORIDE
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 71335-2602-1 | 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71335-2602-1) | 2025-06-05 | | No | Historical |
| 71335-2602-2 | 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71335-2602-2) | 2025-06-05 | | No | Historical |