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Venlafaxine Hydrochloride

NDC 82009-057, Venlafaxine Hydrochloride, capsule, extended release, from QUALLENT PHARMACEUTICALS HEALTH LLC.

Product NDC
82009-057
Status
Listed
Labeler
QUALLENT PHARMACEUTICALS HEALTH LLC
Dosage form
CAPSULE, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA200834
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/82009-057 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • VENLAFAXINE HYDROCHLORIDE75 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
82009-057-10820090057101000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (82009-057-10)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/cb4c04a6-47d1-44ff-8d58-718102fa08eb

  • NADAC price for package 82009005710

    GET /v1/drugs/nadac/82009005710

Use it

Look up 82009-057 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/82009-057 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 82009-057. 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.