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Venlafaxine Hydrochloride

NDC 69367-417, Venlafaxine Hydrochloride, tablet, extended release, from Westminster Pharmaceuticals, LLC.

Product NDC
69367-417
Status
Listed
Labeler
Westminster Pharmaceuticals, LLC
Dosage form
TABLET, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA205468
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/69367-417 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • VENLAFAXINE HYDROCHLORIDE150 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
69367-417-096936704170990 TABLET, EXTENDED RELEASE in 1 BOTTLE (69367-417-09)
69367-417-306936704173030 TABLET, EXTENDED RELEASE in 1 BOTTLE (69367-417-30)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/349308ef-2caf-4fec-b428-56ae06c6771d

  • NADAC price for package 69367041709

    GET /v1/drugs/nadac/69367041709

  • NADAC price for package 69367041730

    GET /v1/drugs/nadac/69367041730

Use it

Look up 69367-417 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/69367-417 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 69367-417. 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.