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Venlafaxine

NDC 70710-1352, Venlafaxine, tablet, extended release, from Zydus Pharmaceuticals USA Inc..

Product NDC
70710-1352
Status
Listed
Labeler
Zydus Pharmaceuticals USA Inc.
Dosage form
TABLET, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA215622
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70710-1352 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • VENLAFAXINE HYDROCHLORIDE225 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
70710-1352-170710135201100 TABLET, EXTENDED RELEASE in 1 BOTTLE (70710-1352-1)
70710-1352-37071013520330 TABLET, EXTENDED RELEASE in 1 BOTTLE (70710-1352-3)
70710-1352-97071013520990 TABLET, EXTENDED RELEASE in 1 BOTTLE (70710-1352-9)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/db1d16b3-d1a2-4f41-adff-a87c17689aa0

  • NADAC price for package 70710135203

    GET /v1/drugs/nadac/70710135203

  • NADAC price for package 70710135209

    GET /v1/drugs/nadac/70710135209

Use it

Look up 70710-1352 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70710-1352 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70710-1352. 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.