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venlafaxine

NDC 46708-434, venlafaxine, tablet, from Alembic Pharmaceuticals Limited.

Product NDC
46708-434
Status
Listed
Labeler
Alembic Pharmaceuticals Limited
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA078932
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/46708-434 \
  -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
46708-434-304670804343030 TABLET in 1 BOTTLE (46708-434-30)
46708-434-3146708043431100 TABLET in 1 BOTTLE (46708-434-31)
46708-434-91467080434911000 TABLET in 1 BOTTLE (46708-434-91)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/b73da6e2-1494-436f-a204-2e4e4c5974b6

Use it

Look up 46708-434 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/46708-434 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 46708-434. 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.