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Hydrochlorothiazide

NDC 65862-134, Hydrochlorothiazide, tablet, from Aurobindo Pharma Limited.

Product NDC
65862-134
Status
Listed
Labeler
Aurobindo Pharma Limited
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA040780
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/65862-134 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • HYDROCHLOROTHIAZIDE50 mg/1

Pharmacologic classes

Increased Diuresis [PE]; Thiazide Diuretic [EPC]; Thiazides [CS]

Package NDCNDC-11Package
65862-134-0165862013401100 TABLET in 1 BOTTLE (65862-134-01)
65862-134-99658620134991000 TABLET in 1 BOTTLE (65862-134-99)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/01f1f478-5493-439f-9b99-f4f82023781c

  • NADAC price for package 65862013401

    GET /v1/drugs/nadac/65862013401

  • NADAC price for package 65862013499

    GET /v1/drugs/nadac/65862013499

Use it

Look up 65862-134 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/65862-134 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 65862-134. 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.