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Miglitol

NDC 69367-305, Miglitol, tablet, coated, from Westminster Pharmaceuticals, LLC.

Product NDC
69367-305
Status
Listed
Labeler
Westminster Pharmaceuticals, LLC
Dosage form
TABLET, COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA203965
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/69367-305 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • MIGLITOL100 mg/1

Pharmacologic classes

alpha Glucosidase Inhibitors [MoA]; alpha-Glucosidase Inhibitor [EPC]

Package NDCNDC-11Package
69367-305-0169367030501100 TABLET, COATED in 1 BOTTLE (69367-305-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/b8da2015-d254-2425-e053-2995a90acf0e

Use it

Look up 69367-305 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/69367-305 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 69367-305. 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.