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venlafaxine

NDC 70518-1385, venlafaxine hydrochloride, tablet, from REMEDYREPACK INC..

Product NDC
70518-1385
Status
Listed
Labeler
REMEDYREPACK INC.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA090555
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70518-1385 \
  -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
70518-1385-07051813850030 TABLET in 1 BLISTER PACK (70518-1385-0)
70518-1385-17051813850190 TABLET in 1 BOTTLE, PLASTIC (70518-1385-1)
70518-1385-37051813850360 TABLET in 1 BOTTLE, PLASTIC (70518-1385-3)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/4a82cef5-693e-46e9-90c4-bff753cdce37

Use it

Look up 70518-1385 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70518-1385 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70518-1385. 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.