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Venlafaxine Hydrochloride

NDC 60760-836, Venlafaxine Hydrochloride, capsule, extended release, from ST. MARY'S MEDICAL PARK PHARMACY.

Product NDC
60760-836
Status
Listed
Labeler
ST. MARY'S MEDICAL PARK PHARMACY
Dosage form
CAPSULE, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA200834
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/60760-836 \
  -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
60760-836-306076008363030 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (60760-836-30)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/35d3148b-52f3-197c-e063-6294a90a44e3

Use it

Look up 60760-836 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/60760-836 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 60760-836. 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.