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VILAZODONE HYDROCHLORIDE

NDC 46708-233, VILAZODONE HYDROCHLORIDE, tablet, film coated, from Alembic Pharmaceuticals Limited.

Product NDC
46708-233
Status
Listed
Labeler
Alembic Pharmaceuticals Limited
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA208202
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/46708-233 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • VILAZODONE HYDROCHLORIDE20 mg/1
Package NDCNDC-11Package
46708-233-304670802333030 TABLET, FILM COATED in 1 BOTTLE (46708-233-30)
46708-233-7146708023371500 TABLET, FILM COATED in 1 BOTTLE (46708-233-71)
46708-233-904670802339090 TABLET, FILM COATED in 1 BOTTLE (46708-233-90)
46708-233-91467080233911000 TABLET, FILM COATED in 1 BOTTLE (46708-233-91)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/0374fbb1-b0fb-4150-b1e7-92e2b0d32ecf

Use it

Look up 46708-233 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/46708-233 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 46708-233. 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.