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venlafaxine hydrochloride

NDC 65841-751, venlafaxine hydrochloride, capsule, extended release, from Zydus Lifesciences Limited.

Product NDC
65841-751
Status
Listed
Labeler
Zydus Lifesciences Limited
Dosage form
CAPSULE, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA090174
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/65841-751 \
  -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
65841-751-066584107510630 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (65841-751-06)
65841-751-10658410751101000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (65841-751-10)
65841-751-166584107511690 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (65841-751-16)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/1be1be3a-304b-4e31-8732-335247029191

Use it

Look up 65841-751 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/65841-751 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 65841-751. 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.