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Hydrochlorothiazide

NDC 69584-362, Hydrochlorothiazide, tablet, from Oxford Pharmaceuticals, LLC.

Product NDC
69584-362
Status
Listed
Labeler
Oxford Pharmaceuticals, LLC
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA087068
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/69584-362 \
  -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
69584-362-1069584036210100 TABLET in 1 BOTTLE (69584-362-10)
69584-362-90695840362901000 TABLET in 1 BOTTLE (69584-362-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/afbb9a0e-c22f-4133-8015-b4b2ab4d32e6

  • NADAC price for package 69584036210

    GET /v1/drugs/nadac/69584036210

  • NADAC price for package 69584036290

    GET /v1/drugs/nadac/69584036290

Use it

Look up 69584-362 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/69584-362 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 69584-362. 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.