Venlafaxine
NDC 70710-1350, Venlafaxine, tablet, extended release, from Zydus Pharmaceuticals USA Inc..
- Product NDC
- 70710-1350
- Status
- Listed
- Labeler
- Zydus Pharmaceuticals USA Inc.
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA215622
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/70710-1350 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- VENLAFAXINE HYDROCHLORIDE150 mg/1
Pharmacologic classes
Norepinephrine Uptake Inhibitors [MoA]; Serotonin Uptake Inhibitors [MoA]; Serotonin and Norepinephrine Reuptake Inhibitor [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 70710-1350-1 | 70710135001 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (70710-1350-1) |
| 70710-1350-3 | 70710135003 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (70710-1350-3) |
| 70710-1350-9 | 70710135009 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (70710-1350-9) |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/db1d16b3-d1a2-4f41-adff-a87c17689aa0NADAC price for package 70710135003
GET /v1/drugs/nadac/70710135003NADAC price for package 70710135009
GET /v1/drugs/nadac/70710135009
Use it
Look up 70710-1350 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/70710-1350 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 70710-1350. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.