Venlafaxine Hydrochloride
NDC 47335-760, Venlafaxine Hydrochloride, tablet, extended release, from Sun Pharmaceutical Industries, Inc..
- Product NDC
- 47335-760
- Status
- Listed
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA091272
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/47335-760 \ -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 |
|---|---|---|
| 47335-760-08 | 47335076008 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-760-08) |
| 47335-760-18 | 47335076018 | 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-760-18) |
| 47335-760-61 | 47335076061 | 10 BLISTER PACK in 1 BOX, UNIT-DOSE (47335-760-61) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK |
| 47335-760-81 | 47335076081 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-760-81) |
| 47335-760-83 | 47335076083 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-760-83) |
| 47335-760-88 | 47335076088 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-760-88) |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/dc989aa7-c4ab-4359-a971-523eb477ef9b
Use it
Look up 47335-760 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/47335-760 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 47335-760. 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.