venlafaxine
- Product NDC
- 71335-1212
- 11-digit product format
- 713351212
- Labeler code
- 71335
- Product ID
- 71335-1212_ad4cde3d-eba4-4f33-ac0f-94fab87a4003
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- venlafaxine hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA090555
- Marketing category
- ANDA
- Marketing start
- 2010-04-07
- Marketing end
- 0000-00-00
- Substance
- VENLAFAXINE HYDROCHLORIDE
- Active strength
- 100 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
- 2020-12-31
- 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 |
|---|
| 71335-1212-1 | 71335121201 | 30 TABLET in 1 BOTTLE (71335-1212-1) | 30 tablet | 2019-05-07 | 0000-00-00 | No | No | Current |
| 71335-1212-2 | 71335121202 | 60 TABLET in 1 BOTTLE (71335-1212-2) | 60 tablet | 2019-05-07 | 0000-00-00 | No | No | Current |
| 71335-1212-3 | 71335121203 | 90 TABLET in 1 BOTTLE (71335-1212-3) | 90 tablet | 2019-05-07 | 0000-00-00 | No | No | Current |
| 71335-1212-4 | 71335121204 | 18 TABLET in 1 BOTTLE (71335-1212-4) | 18 tablet | 2019-05-07 | 0000-00-00 | No | No | Current |