glyburide
NDC 68382-656, glyburide, tablet, from Zydus Pharmaceuticals (USA) Inc..
- Product NDC
- 68382-656
- Status
- Listed
- Labeler
- Zydus Pharmaceuticals (USA) Inc.
- Dosage form
- TABLET
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA206749
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/68382-656 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- GLYBURIDE1.25 mg/1
Pharmacologic classes
Sulfonylurea Compounds [CS]; Sulfonylurea [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 68382-656-01 | 68382065601 | 100 TABLET in 1 BOTTLE (68382-656-01) |
| 68382-656-05 | 68382065605 | 500 TABLET in 1 BOTTLE (68382-656-05) |
| 68382-656-06 | 68382065606 | 30 TABLET in 1 BOTTLE (68382-656-06) |
| 68382-656-10 | 68382065610 | 1000 TABLET in 1 BOTTLE (68382-656-10) |
| 68382-656-16 | 68382065616 | 90 TABLET in 1 BOTTLE (68382-656-16) |
| 68382-656-77 | 68382065677 | 10 BLISTER PACK in 1 CARTON (68382-656-77) / 10 TABLET in 1 BLISTER PACK (68382-656-30) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/87781ea8-62ec-483c-a4dd-8c965ce59485
Use it
Look up 68382-656 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/68382-656 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 68382-656. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.