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Venlafaxine

NDC 70518-4779, Venlafaxine, tablet, from REMEDYREPACK INC..

Product NDC
70518-4779
Status
Listed
Labeler
REMEDYREPACK INC.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA077653
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70518-4779 \
  -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
70518-4779-07051847790030 TABLET in 1 BLISTER PACK (70518-4779-0)

Linked data

RxNorm, label and prices

RxNorm concepts

RxNorm links no concept to this product's packages.

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/407134df-8c44-4321-8af5-0a5b60ca65ac

Use it

Look up 70518-4779 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70518-4779 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70518-4779. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.

Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.