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HYDROCHLOROTHIAZIDE

NDC 70518-3780, hydrochlorothiazide, tablet, from REMEDYREPACK INC..

Product NDC
70518-3780
Status
Listed
Labeler
REMEDYREPACK INC.
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/70518-3780 \
  -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
70518-3780-07051837800090 TABLET in 1 BOTTLE, PLASTIC (70518-3780-0)
70518-3780-17051837800130 TABLET in 1 BLISTER PACK (70518-3780-1)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/1570f1ad-8372-477f-89c3-8c9ce01e27d1

Use it

Look up 70518-3780 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70518-3780 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70518-3780. 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.