venlafaxine
- Product NDC
- 71335-0942
- 11-digit product format
- 713350942
- Labeler code
- 71335
- Product ID
- 71335-0942_88f0d254-cc09-46aa-9da8-4c64759f2eaf
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- venlafaxine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA078932
- Marketing category
- ANDA
- Marketing start
- 2015-10-01
- 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 |
|---|
| 71335-0942-1 | 71335094201 | 30 TABLET in 1 BOTTLE (71335-0942-1) | 30 tablet | 2016-03-01 | 0000-00-00 | No | No | Current |
| 71335-0942-2 | 71335094202 | 60 TABLET in 1 BOTTLE (71335-0942-2) | 60 tablet | 2016-03-01 | 0000-00-00 | No | No | Current |
| 71335-0942-3 | 71335094203 | 90 TABLET in 1 BOTTLE (71335-0942-3) | 90 tablet | 2016-03-01 | 0000-00-00 | No | No | Current |
| 71335-0942-4 | 71335094204 | 10 TABLET in 1 BOTTLE (71335-0942-4) | 10 tablet | 2016-03-01 | 0000-00-00 | No | No | Current |