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Venlafaxine Hydrochloride

NDC 68084-709, Venlafaxine Hydrochloride, capsule, extended release, from American Health Packaging.

Product NDC
68084-709
Status
Listed
Labeler
American Health Packaging
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/68084-709 \
  -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
68084-709-0168084070901100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-709-01) / 1 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (68084-709-11)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/e05bdeb4-07a9-441e-901b-f2aea550db2b

  • NADAC price for package 68084070901

    GET /v1/drugs/nadac/68084070901

Use it

Look up 68084-709 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68084-709 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68084-709. 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.