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Telmisartan and Hydrochlorothiazide

NDC 68462-842, Telmisartan and Hydrochlorothiazide, tablet, from Glenmark Pharmaceuticals Inc., USA.

Product NDC
68462-842
Status
Listed
Labeler
Glenmark Pharmaceuticals Inc., USA
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA202544
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/68462-842 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • TELMISARTAN80 mg/1
  • HYDROCHLOROTHIAZIDE25 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
68462-842-13684620842133 BLISTER PACK in 1 CARTON (68462-842-13) / 10 TABLET in 1 BLISTER PACK

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/1e55800d-f77c-4950-a6d7-2055f4c7ea17

  • NADAC price for package 68462084213

    GET /v1/drugs/nadac/68462084213

Use it

Look up 68462-842 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68462-842 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68462-842. 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.