NDC 68382-655-30 - glyburide and metformin 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
- 68382-655
- Requested NDC
- 68382-655-30
- Package NDCs from labels
- 68382-655-06, 68382-655-16, 68382-655-01, 68382-655-05, 68382-655-10, 68382-655-30, 68382-655-77
- Manufacturer
- Zydus Pharmaceuticals (USA) Inc.
- Effective date
- 2026-06-10
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| glyburide and metformin hydrochloride - Zydus Pharmaceuticals (USA) Inc. | Zydus Pharmaceuticals (USA) Inc. | 2026-06-10 | HUMAN PRESCRIPTION DRUG LABEL |
| glyburide and metformin hydrochloride - Bryant Ranch Prepack | Bryant Ranch Prepack | 2021-12-27 | HUMAN PRESCRIPTION DRUG LABEL |
| Glyburide and Metformin Hydrochloride Tablets, USP Rx only | Preferred Pharmaceuticals Inc. | 2020-06-08 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 68382-655-01 | glyburide and metformin hydrochloride | 100 in 1 BOTTLE | TABLET | 100 | 6 | |
| 68382-655-05 | glyburide and metformin hydrochloride | 500 in 1 BOTTLE | TABLET | 500 | 6 | |
| 68382-655-06 | glyburide and metformin hydrochloride | 30 in 1 BOTTLE | TABLET | 30 | 6 | |
| 68382-655-10 | glyburide and metformin hydrochloride | 1000 in 1 BOTTLE | TABLET | 1000 | 6 | |
| 68382-655-16 | glyburide and metformin hydrochloride | 90 in 1 BOTTLE | TABLET | 90 | 6 | |
| 68382-655-30 | glyburide and metformin hydrochloride | 10 in 1 BLISTER PACK | TABLET | 10 | 6 | |
| 68382-655-77 | glyburide and metformin hydrochloride | 10 in 1 CARTON | TABLET | 10 | 6 |
DailyMed Dashboard NDC Coverage#
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.