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GLYBURIDE

NDC 50090-0495, GLYBURIDE, tablet, from A-S Medication Solutions.

Product NDC
50090-0495
Status
Listed
Labeler
A-S Medication Solutions
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA090937
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/50090-0495 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • GLYBURIDE5 mg/1

Pharmacologic classes

Sulfonylurea Compounds [CS]; Sulfonylurea [EPC]

Package NDCNDC-11Package
50090-0495-05009004950030 TABLET in 1 BOTTLE (50090-0495-0)
50090-0495-150090049501100 TABLET in 1 BOTTLE (50090-0495-1)
50090-0495-25009004950260 TABLET in 1 BOTTLE (50090-0495-2)
50090-0495-850090049508200 TABLET in 1 BOTTLE (50090-0495-8)
50090-0495-95009004950990 TABLET in 1 BOTTLE (50090-0495-9)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/3c91a408-973b-4572-832f-515f61d5be1f

Use it

Look up 50090-0495 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/50090-0495 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 50090-0495. 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.