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Chlorothiazide sodium

NDC 68083-614, Chlorothiazide sodium, injection, powder, lyophilized, for solution, from Gland Pharma Limited.

Product NDC
68083-614
Status
Listed
Labeler
Gland Pharma Limited
Dosage form
INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Route
INTRAVENOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA218630
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/68083-614 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • CHLOROTHIAZIDE SODIUM500 mg/18mL

Pharmacologic classes

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

Package NDCNDC-11Package
68083-614-01680830614011 VIAL in 1 CARTON (68083-614-01) / 18 mL in 1 VIAL

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/bf921935-9740-458e-b786-69f76d8ad139

Use it

Look up 68083-614 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68083-614 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68083-614. 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.