VENLAFAXINE
NDC 71209-026, venlafaxine, tablet, from Cadila Pharmaceuticals Limited.
- Product NDC
- 71209-026
- Status
- Listed
- Labeler
- Cadila Pharmaceuticals Limited
- Dosage form
- TABLET
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA206250
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/71209-026 \ -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 NDC | NDC-11 | Package |
|---|---|---|
| 71209-026-05 | 71209002605 | 100 TABLET in 1 BOTTLE (71209-026-05) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/2ed61dcf-42e3-47cf-a607-459eef5fea98
Use it
Look up 71209-026 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/71209-026 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 71209-026. 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.