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Telmisartan and Hydrochlorothiazide

NDC 62332-210, Telmisartan and Hydrochlorothiazide, tablet, from Alembic Pharmaceuticals Inc..

Product NDC
62332-210
Status
Listed
Labeler
Alembic Pharmaceuticals Inc.
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/62332-210 \
  -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
62332-210-1062332021010100 TABLET in 1 CARTON (62332-210-10)
62332-210-306233202103030 TABLET in 1 BOTTLE (62332-210-30)
62332-210-91623320210911000 TABLET in 1 BOTTLE (62332-210-91)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/e80f232c-c1c4-4524-a0a5-d23ee0d1f3b7

  • NADAC price for package 62332021030

    GET /v1/drugs/nadac/62332021030

Use it

Look up 62332-210 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/62332-210 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 62332-210. 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.