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CHLORTHALIDONE CHLORTHALIDONE

NDC 46708-676, CHLORTHALIDONE, tablet, from Alembic Pharmaceuticals Limited.

Product NDC
46708-676
Status
Listed
Labeler
Alembic Pharmaceuticals Limited
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA216262
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/46708-676 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • CHLORTHALIDONE25 mg/1

Pharmacologic classes

Increased Diuresis [PE]; Thiazide-like Diuretic [EPC]

Package NDCNDC-11Package
46708-676-3146708067631100 TABLET in 1 BOTTLE (46708-676-31)
46708-676-904670806769090 TABLET in 1 BOTTLE (46708-676-90)
46708-676-91467080676911000 TABLET in 1 BOTTLE (46708-676-91)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/1b98d1a1-9d3d-41d2-a5e9-744b851d30d4

Use it

Look up 46708-676 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/46708-676 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 46708-676. 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.