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venlafaxine hydrochloride

NDC 68382-035, venlafaxine hydrochloride, capsule, extended release, from Zydus Pharmaceuticals USA Inc..

Product NDC
68382-035
Status
Listed
Labeler
Zydus Pharmaceuticals USA Inc.
Dosage form
CAPSULE, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA090174
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/68382-035 \
  -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
68382-035-066838200350630 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68382-035-06)
68382-035-10683820035101000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68382-035-10)
68382-035-166838200351690 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68382-035-16)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/5351fe67-17d9-42ec-9e8b-6585fdb9e29e

  • NADAC price for package 68382003510

    GET /v1/drugs/nadac/68382003510

  • NADAC price for package 68382003516

    GET /v1/drugs/nadac/68382003516

Use it

Look up 68382-035 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68382-035 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68382-035. 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.