Venlafaxine Hydrochloride
NDC 67046-0390, Venlafaxine Hydrochloride, capsule, extended release, from Coupler LLC.
- Product NDC
- 67046-0390
- Status
- Listed
- Labeler
- Coupler LLC
- Dosage form
- CAPSULE, EXTENDED RELEASE
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA200834
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/67046-0390 \ -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 |
|---|---|---|
| 67046-0390-3 | 67046039003 | 30 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (67046-0390-3) |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/5358f20f-b864-0aae-e063-6394a90a7eab
Use it
Look up 67046-0390 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/67046-0390 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 67046-0390. 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.