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VENLAFAXINE HYDROCHLORIDE

NDC 68001-496, venlafaxine, tablet, extended release, from BluePoint Laboratories.

Product NDC
68001-496
Status
Listed
Labeler
BluePoint Laboratories
Dosage form
TABLET, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA214419
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/68001-496 \
  -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
68001-496-046800104960430 TABLET, EXTENDED RELEASE in 1 BOTTLE (68001-496-04)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/5efe1336-c796-4560-8110-a64c80eefb0c

  • NADAC price for package 68001049604

    GET /v1/drugs/nadac/68001049604

Use it

Look up 68001-496 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68001-496 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68001-496. 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.