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Venlafaxine Hydrochloride

NDC 50771-005, venlafaxine hydrochloride, tablet, from Yaopharma Co., Ltd..

Product NDC
50771-005
Status
Listed
Labeler
Yaopharma Co., Ltd.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA202036
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/50771-005 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • VENLAFAXINE HYDROCHLORIDE100 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
50771-005-0250771000502100 TABLET in 1 BOTTLE, PLASTIC (50771-005-02)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/38fd2c97-cd30-2f7d-e054-00144ff8d46c

Use it

Look up 50771-005 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/50771-005 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 50771-005. 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.