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Venlafaxine

NDC 68382-101, Venlafaxine, tablet, from Zydus Pharmaceuticals USA Inc..

Product NDC
68382-101
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/68382-101 \
  -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
68382-101-0168382010101100 TABLET in 1 BOTTLE (68382-101-01)
68382-101-0568382010105500 TABLET in 1 BOTTLE (68382-101-05)
68382-101-066838201010630 TABLET in 1 BOTTLE (68382-101-06)
68382-101-10683820101101000 TABLET in 1 BOTTLE (68382-101-10)
68382-101-146838201011460 TABLET in 1 BOTTLE (68382-101-14)
68382-101-166838201011690 TABLET in 1 BOTTLE (68382-101-16)

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 68382010101

    GET /v1/drugs/nadac/68382010101

Use it

Look up 68382-101 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68382-101 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68382-101. 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.