Venlafaxine
- Product NDC
- 71335-0383
- 11-digit product format
- 713350383
- Labeler code
- 71335
- Product ID
- 71335-0383_4854eb5c-3338-45c7-b38f-5443a67edbda
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Venlafaxine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA202036
- Marketing category
- ANDA
- Marketing start
- 2016-04-19
- Marketing end
- 0000-00-00
- Substance
- VENLAFAXINE HYDROCHLORIDE
- Active strength
- 38 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
- 2021-12-31
- 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 |
|---|
| 71335-0383-1 | 71335038301 | 30 TABLET in 1 BOTTLE (71335-0383-1) | 30 tablet | 2017-04-14 | 0000-00-00 | No | No | Current |
| 71335-0383-2 | 71335038302 | 60 TABLET in 1 BOTTLE (71335-0383-2) | 60 tablet | 2017-04-14 | 0000-00-00 | No | No | Current |
| 71335-0383-3 | 71335038303 | 90 TABLET in 1 BOTTLE (71335-0383-3) | 90 tablet | 2017-04-14 | 0000-00-00 | No | No | Current |
| 71335-0383-4 | 71335038304 | 10 TABLET in 1 BOTTLE (71335-0383-4) | 10 tablet | 2017-04-14 | 0000-00-00 | No | No | Current |