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VENLAFAXINE

NDC 71209-027, venlafaxine, tablet, from Cadila Pharmaceuticals Limited.

Product NDC
71209-027
Status
Listed
Labeler
Cadila Pharmaceuticals Limited
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA206250
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71209-027 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • VENLAFAXINE HYDROCHLORIDE50 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
71209-027-0571209002705100 TABLET in 1 BOTTLE (71209-027-05)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/2ed61dcf-42e3-47cf-a607-459eef5fea98

Use it

Look up 71209-027 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71209-027 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71209-027. 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.