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HYDROCHLOROTHIAZIDE

NDC 69315-155, HYDROCHLOROTHIAZIDE, tablet, from Leading Pharma, LLC.

Product NDC
69315-155
Status
Listed
Labeler
Leading Pharma, LLC
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA040702
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/69315-155 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • HYDROCHLOROTHIAZIDE12.5 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
69315-155-0169315015501100 TABLET in 1 BOTTLE, PLASTIC (69315-155-01)
69315-155-10693150155101000 TABLET in 1 BOTTLE, PLASTIC (69315-155-10)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/8c868894-667e-4a51-906a-838d63e420ba

  • NADAC price for package 69315015501

    GET /v1/drugs/nadac/69315015501

  • NADAC price for package 69315015510

    GET /v1/drugs/nadac/69315015510

Use it

Look up 69315-155 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/69315-155 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 69315-155. 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.