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Telmisartan and Hydrochlorothiazide

NDC 46708-210, Telmisartan and Hydrochlorothiazide, tablet, from Alembic Pharmaceuticals Limited.

Product NDC
46708-210
Status
Listed
Labeler
Alembic Pharmaceuticals Limited
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA203010
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/46708-210 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • TELMISARTAN80 mg/1
  • HYDROCHLOROTHIAZIDE12.5 mg/1

Pharmacologic classes

Angiotensin 2 Receptor Antagonists [MoA]; Angiotensin 2 Receptor Blocker [EPC]; Increased Diuresis [PE]; Thiazide Diuretic [EPC]; Thiazides [CS]

Package NDCNDC-11Package
46708-210-1046708021010100 TABLET in 1 CARTON (46708-210-10)
46708-210-304670802103030 TABLET in 1 BOTTLE (46708-210-30)
46708-210-91467080210911000 TABLET in 1 BOTTLE (46708-210-91)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/5b476740-e3f0-4f68-b07c-cd9eb2fa27ca

Use it

Look up 46708-210 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/46708-210 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 46708-210. 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.