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VENLAFAXINE HYDROCHLORIDE

NDC 72865-197, venlafaxine, tablet, extended release, from XLCare Pharmaceuticals, Inc..

Product NDC
72865-197
Status
Listed
Labeler
XLCare Pharmaceuticals, Inc.
Dosage form
TABLET, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA214419
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/72865-197 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • VENLAFAXINE HYDROCHLORIDE37.5 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
72865-197-307286501973030 TABLET, EXTENDED RELEASE in 1 BOTTLE (72865-197-30)
72865-197-907286501979090 TABLET, EXTENDED RELEASE in 1 BOTTLE (72865-197-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/68f40801-d35e-464e-ac94-21016b617ea2

Use it

Look up 72865-197 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/72865-197 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 72865-197. 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.