Venlafaxine Hydrochloride
- Product NDC
- 0093-7381
- 11-digit product format
- 000937381
- Labeler code
- 0093
- Product ID
- 0093-7381_1549b126-edc2-4bf0-b78d-be985b07db95
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Venlafaxine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Teva Pharmaceuticals USA, Inc.
- Application
- ANDA076690
- Marketing category
- ANDA
- Marketing start
- 2006-08-04
- Marketing end
- 2021-04-30
- Substance
- VENLAFAXINE HYDROCHLORIDE
- Active strength
- 50 mg/1
- Pharmacologic classes
- Norepinephrine Uptake Inhibitors [MoA],Serotonin and Norepinephrine Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0093-7381-01 | 00093738101 | 100 TABLET in 1 BOTTLE (0093-7381-01) | 100 tablet | 2006-08-04 | 2021-04-30 | No | No | Current |