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Venlafaxine

NDC 70771-1652, Venlafaxine, tablet, extended release, from Zydus Lifesciences Limited.

Product NDC
70771-1652
Status
Listed
Labeler
Zydus Lifesciences Limited
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/70771-1652 \
  -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
70771-1652-170771165201100 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1652-1)
70771-1652-37077116520330 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1652-3)
70771-1652-97077116520990 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1652-9)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/750333ce-a512-42e1-b9e3-179714b488df

Use it

Look up 70771-1652 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70771-1652 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70771-1652. 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.