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Miglitol

NDC 71205-935, Miglitol, tablet, coated, from Proficient Rx LP.

Product NDC
71205-935
Status
Listed
Labeler
Proficient Rx LP
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/71205-935 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • MIGLITOL25 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
71205-935-0071205093500100 TABLET, COATED in 1 BOTTLE (71205-935-00)
71205-935-307120509353030 TABLET, COATED in 1 BOTTLE (71205-935-30)
71205-935-607120509356060 TABLET, COATED in 1 BOTTLE (71205-935-60)
71205-935-907120509359090 TABLET, COATED in 1 BOTTLE (71205-935-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/f16ecb50-e54e-43e1-8789-eaf5bc94f332

Use it

Look up 71205-935 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71205-935 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71205-935. 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.