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Venlafaxine Hydrochloride

NDC 70518-4065, Venlafaxine, tablet, extended release, from REMEDYREPACK INC..

Product NDC
70518-4065
Status
Listed
Labeler
REMEDYREPACK INC.
Dosage form
TABLET, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA216044
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70518-4065 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • VENLAFAXINE HYDROCHLORIDE75 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
70518-4065-07051840650090 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-4065-0)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/9df3a51c-1b89-4d2a-8f41-3755910e9bfb

Use it

Look up 70518-4065 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70518-4065 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70518-4065. 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.