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Venlafaxine Hydrochloride

NDC 42708-194, Venlafaxine Hydrochloride, capsule, extended release, from QPharma, Inc..

Product NDC
42708-194
Status
Listed
Labeler
QPharma, Inc.
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/42708-194 \
  -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
42708-194-304270801943030 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (42708-194-30)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/4992698e-5d5a-6468-e063-6394a90ab404

Use it

Look up 42708-194 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/42708-194 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 42708-194. 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.