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HYDROCHLOROTHIAZIDE

NDC 51655-272, hydrochlorothiazide, tablet, from Northwind Health Company, LLC.

Product NDC
51655-272
Status
Listed
Labeler
Northwind Health Company, LLC
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA085182
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/51655-272 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • HYDROCHLOROTHIAZIDE25 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
51655-272-265165502722690 TABLET in 1 BOTTLE, PLASTIC (51655-272-26)
51655-272-525165502725230 TABLET in 1 BOTTLE, PLASTIC (51655-272-52)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/c8c79657-a09a-bdb6-e053-2995a90ab673

Use it

Look up 51655-272 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/51655-272 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 51655-272. 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.