Venlafaxine Hydrochloride
NDC 70771-1837, Venlafaxine Hydrochloride, capsule, extended release, from Zydus Lifesciences Limited.
- Product NDC
- 70771-1837
- Status
- Listed
- Labeler
- Zydus Lifesciences Limited
- Dosage form
- CAPSULE, EXTENDED RELEASE
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA090174
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/70771-1837 \ -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 |
|---|---|---|
| 70771-1837-0 | 70771183700 | 1000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (70771-1837-0) |
| 70771-1837-3 | 70771183703 | 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (70771-1837-3) |
| 70771-1837-4 | 70771183704 | 10 BLISTER PACK in 1 CARTON (70771-1837-4) / 10 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (70771-1837-2) |
| 70771-1837-5 | 70771183705 | 500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (70771-1837-5) |
| 70771-1837-9 | 70771183709 | 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (70771-1837-9) |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/1349bace-d2cb-4c8f-8cbd-c09e67a2ca1b
Use it
Look up 70771-1837 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/70771-1837 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 70771-1837. 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.