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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Metformin Hydrochloride | METFORMIN HYDROCHLORIDE | Northwind Health Company, LLC | dae7b1c1-7ff1-883c-e053-2a95a90a1a2b | 2026-01-01 | Boxed warning, Warnings, Adverse reactions | 786Z46389E |
| Glyburide and Metformin Hydrochloride | GLYBURIDE AND METFORMIN HYDROCHLORIDE | Northwind Health Company, LLC | adb751e0-19f6-3f41-e053-2a95a90a2df8 | 2026-01-01 | Boxed warning, Warnings, Adverse reactions | 861753 786Z46389E SX6K58TVWC |
| Metformin Hydrochloride | METFORMIN HYDROCHLORIDE | Northwind Health Company, LLC | f2a27d7a-ade4-421f-e053-2a95a90a01a9 | 2026-01-01 | Boxed warning, Warnings, Adverse reactions | 786Z46389E |
| GLYBURIDE | GLYBURIDE | Northwind Health Company, LLC | d9cb9251-7b31-72a0-e053-2a95a90a4315 | 2026-01-01 | Adverse reactions | SX6K58TVWC |
| METFORMIN HYDROCHLORIDE | METFORMIN HYDROCHLORIDE | Northwind Health Company, LLC | 07d8a69f-30d9-7511-e063-6394a90a95ca | 2026-01-01 | Boxed warning, Warnings, Adverse reactions | 786Z46389E |
| Metformin Hydrochloride | METFORMIN HYDROCHLORIDE | Northwind Health Company, LLC | 0178b9dd-bafa-9e81-e063-6294a90a88b0 | 2026-01-01 | Boxed warning, Warnings, Adverse reactions | 786Z46389E |
| GLYBURIDE | GLYBURIDE | Northwind Health Company, LLC | db47a517-f8bb-136f-e053-2a95a90ad8c5 | 2026-01-01 | Adverse reactions | SX6K58TVWC |
| Metformin Hydrochloride | METFORMIN HYDROCHLORIDE | Northwind Health Company, LLC | f5ef117c-27ff-c21e-e053-2995a90ae145 | 2026-01-01 | Boxed warning, Warnings, Adverse reactions | 786Z46389E |
| Metformin Hydrochloride | METFORMIN HYDROCHLORIDE | Northwind Health Company, LLC | db113f46-6fac-9005-e053-2995a90a017a | 2026-01-01 | Boxed warning, Warnings, Adverse reactions | 786Z46389E |
| METFORMIN HYDROCHLORIDE EXTENDED RELEASE | METFORMIN HYDROCHLORIDE | Northwind Health Company, LLC | 4e5a19c6-6ac6-ffc0-e063-6394a90a9827 | 2026-01-01 | Boxed warning, Warnings, Adverse reactions | 786Z46389E |
| NUTRALOX | CALCIUM CARBONATE | HART Health | 3941b84e-3b4b-46eb-851b-979bac1ae997 | 2025-12-31 | Warnings | H0G9379FGK |
| Youth Glow Vitamin C CC Cream Sunscreen SPF 50 - Fair | OCTINOXATE, TITANIUM DIOXIDE, ZINC OXIDE | Pur-lisse Beauty, LLC | 47428cd4-fbad-ba7a-e063-6394a90a1c5c | 2025-12-31 | Warnings | 15FIX9V2JP |
| Youth Glow Vitamin C CC Cream Sunscreen SPF 50 - Medium | OCTINOXATE, TITANIUM DIOXIDE, ZINC OXIDE | Pur-lisse Beauty, LLC | 47433a62-91e0-b031-e063-6294a90a0d49 | 2025-12-31 | Warnings | 15FIX9V2JP |
| Radiant Glow Illuminating BB Cream Sunscreen SPF 30 - Fair | OCTINOXATE, TITANIUM DIOXIDE, ZINC OXIDE | Pur-lisse Beauty, LLC | 4743b6a9-4d79-1b2b-e063-6394a90a9710 | 2025-12-31 | Warnings | 15FIX9V2JP |
| Radiant Glow Illuminating BB Cream Sunscreen SPF 30 - Light Medium | OCTINOXATE, TITANIUM DIOXIDE, ZINC OXIDE | Pur-lisse Beauty, LLC | 4744e501-f12a-6d25-e063-6394a90a2574 | 2025-12-31 | Warnings | 15FIX9V2JP |
| Radiant Glow Illuminating BB Cream Sunscreen SPF 30 - Medium | OCTINOXATE, TITANIUM DIOXIDE, ZINC OXIDE | Pur-lisse Beauty, LLC | 47456bf5-9f6c-e6a5-e063-6294a90a7054 | 2025-12-31 | Warnings | 15FIX9V2JP |
| Radiant Glow Illuminating BB Cream Sunscreen SPF 30 - Tan | OCTINOXATE, TITANIUM DIOXIDE, ZINC OXIDE | Pur-lisse Beauty, LLC | 4745ab56-abaa-42de-e063-6394a90a6310 | 2025-12-31 | Warnings | 15FIX9V2JP |
| Radiant Glow Illuminating BB Cream Sunscreen SPF 30 - Tan Deep | OCTINOXATE, TITANIUM DIOXIDE, ZINC OXIDE | Pur-lisse Beauty, LLC | 4745ebec-acb0-77c4-e063-6394a90aee07 | 2025-12-31 | Warnings | 15FIX9V2JP |
| Radiant Glow Illuminating BB Cream Sunscreen SPF 30 - Deep | OCTINOXATE, TITANIUM DIOXIDE, ZINC OXIDE | Pur-lisse Beauty, LLC | 47461ad3-a11e-2a11-e063-6294a90a0f8f | 2025-12-31 | Warnings | 15FIX9V2JP |
| Dermagesic | PRAMOXINE HCL, ZINC OXIDE, CALAMINE | Llorens Pharmaceutical International Division | bbff6b53-29da-45c1-8ccd-3e9df7f250e0 | 2025-12-31 | Warnings | 1K09F3G675 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.