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venlafaxine

NDC 46708-430, venlafaxine, tablet, from Alembic Pharmaceuticals Limited.

Product NDC
46708-430
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/46708-430 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • VENLAFAXINE HYDROCHLORIDE25 mg/1

Pharmacologic classes

Norepinephrine Uptake Inhibitors [MoA]; Serotonin Uptake Inhibitors [MoA]; Serotonin and Norepinephrine Reuptake Inhibitor [EPC]

Package NDCNDC-11Package
46708-430-304670804303030 TABLET in 1 BOTTLE (46708-430-30)
46708-430-3146708043031100 TABLET in 1 BOTTLE (46708-430-31)
46708-430-91467080430911000 TABLET in 1 BOTTLE (46708-430-91)

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 46708-430 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/46708-430 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 46708-430. 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.