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HYDROCHLOROTHIAZIDE

NDC 68071-3652, HYDROCHLOROTHIAZIDE, tablet, from NuCare Pharmaceuticals,Inc..

Product NDC
68071-3652
Status
Listed
Labeler
NuCare Pharmaceuticals,Inc.
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/68071-3652 \
  -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
68071-3652-168071365201100 TABLET in 1 BOTTLE, PLASTIC (68071-3652-1)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/1e02787f-ccb5-abc2-e063-6294a90af7c3

Use it

Look up 68071-3652 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68071-3652 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68071-3652. 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.