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Tiagabine Hydrochloride

NDC 72205-087, Tiagabine Hydrochloride, tablet, from Novadoz Pharmaceuticals LLC.

Product NDC
72205-087
Status
Listed
Labeler
Novadoz Pharmaceuticals LLC
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA214816
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/72205-087 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • TIAGABINE HYDROCHLORIDE16 mg/1

Pharmacologic classes

Anti-epileptic Agent [EPC]; Decreased Central Nervous System Disorganized Electrical Activity [PE]

Package NDCNDC-11Package
72205-087-307220500873030 TABLET in 1 BOTTLE (72205-087-30)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/7c034fe0-cdac-49e1-8e39-592846ea3bec

Use it

Look up 72205-087 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/72205-087 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 72205-087. 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.