Glipizide
NDC 71335-1031, Glipizide, tablet, film coated, extended release, from Bryant Ranch Prepack.
- Product NDC
- 71335-1031
- Status
- Listed
- Labeler
- Bryant Ranch Prepack
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA204720
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/71335-1031 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- GLIPIZIDE5 mg/1
Pharmacologic classes
Sulfonylurea Compounds [CS]; Sulfonylurea [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 71335-1031-1 | 71335103101 | 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1031-1) |
| 71335-1031-2 | 71335103102 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1031-2) |
| 71335-1031-3 | 71335103103 | 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1031-3) |
| 71335-1031-4 | 71335103104 | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1031-4) |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/0338aff9-29f9-405e-b516-06ef4b863863
Use it
Look up 71335-1031 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/71335-1031 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 71335-1031. 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.