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Venlafaxine

NDC 68382-019, Venlafaxine, tablet, from Zydus Pharmaceuticals USA Inc..

Product NDC
68382-019
Status
Listed
Labeler
Zydus Pharmaceuticals USA Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA077653
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/68382-019 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • VENLAFAXINE HYDROCHLORIDE37.5 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
68382-019-0168382001901100 TABLET in 1 BOTTLE (68382-019-01)
68382-019-0568382001905500 TABLET in 1 BOTTLE (68382-019-05)
68382-019-066838200190630 TABLET in 1 BOTTLE (68382-019-06)
68382-019-10683820019101000 TABLET in 1 BOTTLE (68382-019-10)
68382-019-146838200191460 TABLET in 1 BOTTLE (68382-019-14)
68382-019-166838200191690 TABLET in 1 BOTTLE (68382-019-16)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/72efad5f-0909-46a5-aa13-ac24fe015fe6

  • NADAC price for package 68382001901

    GET /v1/drugs/nadac/68382001901

Use it

Look up 68382-019 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68382-019 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68382-019. 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.