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venlafaxine

NDC 57237-172, venlafaxine hydrochloride, tablet, from Rising Pharma Holdings, Inc..

Product NDC
57237-172
Status
Listed
Labeler
Rising Pharma Holdings, Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA090555
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/57237-172 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • VENLAFAXINE HYDROCHLORIDE25 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
57237-172-0157237017201100 TABLET in 1 BOTTLE (57237-172-01)
57237-172-905723701729090 TABLET in 1 BOTTLE (57237-172-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/20319949-ccf9-477a-a6e3-53502772deb9

  • NADAC price for package 57237017201

    GET /v1/drugs/nadac/57237017201

Use it

Look up 57237-172 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/57237-172 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 57237-172. 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.