NDC 67877-641-33 - lurasidone 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
- 67877-641
- Requested NDC
- 67877-641-33
- Package NDCs from labels
- 67877-641-30, 67877-641-90, 67877-641-05, 67877-641-33, 67877-641-38
- Manufacturer
- Major Pharmaceuticals
- Effective date
- 2025-09-11
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| lurasidone hydrochloride - Major Pharmaceuticals | Major Pharmaceuticals | 2025-09-11 | HUMAN PRESCRIPTION DRUG LABEL |
| Lurasidone Hydrochloride - American Health Packaging | American Health Packaging | 2025-01-02 | HUMAN PRESCRIPTION DRUG LABEL |
| lurasidone hydrochloride - Ascend Laboratories, LLC | Alkem Laboratories Limited | Ascend Laboratories, LLC | Alkem Laboratories Limited | 2023-01-06 | Human Prescription Drug Label |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 67877-641-05 | lurasidone hydrochloride | 500 in 1 BOTTLE | TABLET, FILM COATED | 500 | 8 | |
| 67877-641-30 | lurasidone hydrochloride | 30 in 1 BOTTLE | TABLET, FILM COATED | 30 | 8 | |
| 67877-641-33 | lurasidone hydrochloride | 10 in 1 BLISTER PACK | TABLET, FILM COATED | 10 | 8 | |
| 67877-641-38 | lurasidone hydrochloride | 10 in 1 CARTON | TABLET, FILM COATED | 10 | 8 | |
| 67877-641-90 | lurasidone hydrochloride | 90 in 1 BOTTLE | TABLET, FILM COATED | 90 | 8 |
DailyMed Dashboard NDC Coverage#
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 67877-641-30 | EA - Each | 67877-641 | c748ddee-87a8-4047-b119-d3feb69ceea3 | 1 | 2023-02-06 |
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.