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Venlafaxine Hydrochloride

NDC 0093-9157, Venlafaxine Hydrochloride, tablet, from Teva Pharmaceuticals USA, Inc..

Product NDC
0093-9157
Status
Listed
Labeler
Teva Pharmaceuticals USA, Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA076690
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/0093-9157 \
  -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
0093-9157-0100093915701100 TABLET in 1 BOTTLE (0093-9157-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/37aaa8ac-4e0c-4e04-98b5-19b0d90d857c

  • NADAC price for package 00093915701

    GET /v1/drugs/nadac/00093915701

Use it

Look up 0093-9157 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0093-9157 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0093-9157. 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.