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Venlafaxine Hydrochloride

NDC 47335-759, Venlafaxine Hydrochloride, tablet, extended release, from Sun Pharmaceutical Industries, Inc..

Product NDC
47335-759
Status
Listed
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
TABLET, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA091272
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/47335-759 \
  -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
47335-759-0847335075908100 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-759-08)
47335-759-18473350759181000 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-759-18)
47335-759-614733507596110 BLISTER PACK in 1 BOX, UNIT-DOSE (47335-759-61) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
47335-759-814733507598190 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-759-81)
47335-759-834733507598330 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-759-83)
47335-759-8847335075988100 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-759-88)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/dc989aa7-c4ab-4359-a971-523eb477ef9b

Use it

Look up 47335-759 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/47335-759 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 47335-759. 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.