NDC 68382-596-30 - diltiazem hydrochloride
This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
- Product NDC
- 68382-596
- Requested NDC
- 68382-596-30
- Package NDCs from labels
- 68382-596-06, 68382-596-16, 68382-596-01, 68382-596-05, 68382-596-30, 68382-596-77
- Manufacturer
- Bryant Ranch Prepack
- Effective date
- 2025-06-11
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| diltiazem hydrochloride - Bryant Ranch Prepack | Bryant Ranch Prepack | 2025-06-11 | HUMAN PRESCRIPTION DRUG LABEL |
| DILTIAZEM - Zydus Pharmaceuticals (USA) Inc. | Zydus Lifesciences Limited | Zydus Pharmaceuticals (USA) Inc. | Zydus Lifesciences Limited | 2025-05-01 | HUMAN PRESCRIPTION DRUG LABEL |
| Diltiazem Hydrochloride Extended-Release Capsules, USP Once-A-Day Dosage Rx only | REMEDYREPACK INC. | 2019-05-14 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 68382-596-01 | diltiazem hydrochloride | 100 in 1 BOTTLE | CAPSULE, EXTENDED RELEASE | 100 | 6 | |
| 68382-596-05 | diltiazem hydrochloride | 500 in 1 BOTTLE | CAPSULE, EXTENDED RELEASE | 500 | 6 | |
| 68382-596-06 | diltiazem hydrochloride | 30 in 1 BOTTLE | CAPSULE, EXTENDED RELEASE | 30 | 6 | |
| 68382-596-16 | diltiazem hydrochloride | 90 in 1 BOTTLE | CAPSULE, EXTENDED RELEASE | 90 | 6 | |
| 68382-596-30 | diltiazem hydrochloride | 10 in 1 BLISTER PACK | CAPSULE, EXTENDED RELEASE | 10 | 6 | |
| 68382-596-77 | diltiazem hydrochloride | 10 in 1 CARTON | CAPSULE, EXTENDED RELEASE | 10 | 6 |
DailyMed Dashboard NDC Coverage#
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 68382-596-05 | EA - Each | 68382-596 | 71e70fa7-03c8-4b8d-b864-d94b024bfb64 | 1 | 2019-01-24 |
| 68382-596-16 | EA - Each | 68382-596 | 738bf98e-307a-42b8-91ff-28dc18114543 | 1 | 2018-12-13 |
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.