Venlafaxine Hydrochloride
NDC 70518-4151, VENLAFAXINE HYDROCHLORIDE, capsule, extended release, from REMEDYREPACK INC..
- Product NDC
- 70518-4151
- Status
- Listed
- Labeler
- REMEDYREPACK INC.
- Dosage form
- CAPSULE, EXTENDED RELEASE
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA214654
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/70518-4151 \ -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 NDC | NDC-11 | Package |
|---|---|---|
| 70518-4151-0 | 70518415100 | 30 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (70518-4151-0) |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/33b39416-7981-46fb-ba31-e933a6afcf8b
Use it
Look up 70518-4151 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/70518-4151 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 70518-4151. 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.