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Venlafaxine

NDC 57664-395, Venlafaxine, tablet, from Sun Pharmaceutical Industries, Inc..

Product NDC
57664-395
Status
Listed
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA078627
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/57664-395 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • VENLAFAXINE HYDROCHLORIDE75 mg/1

Pharmacologic classes

Norepinephrine Uptake Inhibitors [MoA]; Serotonin Uptake Inhibitors [MoA]; Serotonin and Norepinephrine Reuptake Inhibitor [EPC]

Package NDCNDC-11Package
57664-395-8857664039588100 TABLET in 1 BOTTLE (57664-395-88)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/55889b3d-74c9-4638-9a14-6a4ca3a99f7f

  • NADAC price for package 57664039588

    GET /v1/drugs/nadac/57664039588

Use it

Look up 57664-395 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/57664-395 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 57664-395. 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.