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glyburide

NDC 65841-832, glyburide, tablet, from Zydus Lifesciences Limited.

Product NDC
65841-832
Status
Listed
Labeler
Zydus Lifesciences Limited
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA206749
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/65841-832 \
  -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 NDCNDC-11Package
65841-832-0165841083201100 TABLET in 1 BOTTLE (65841-832-01)
65841-832-0565841083205500 TABLET in 1 BOTTLE (65841-832-05)
65841-832-066584108320630 TABLET in 1 BOTTLE (65841-832-06)
65841-832-10658410832101000 TABLET in 1 BOTTLE (65841-832-10)
65841-832-166584108321690 TABLET in 1 BOTTLE (65841-832-16)
65841-832-776584108327710 BLISTER PACK in 1 CARTON (65841-832-77) / 10 TABLET in 1 BLISTER PACK (65841-832-30)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/5d0e406f-285d-4716-8971-82f665345517

Use it

Look up 65841-832 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/65841-832 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 65841-832. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
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Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.