Venlafaxine Hydrochloride
- Product NDC
- 63629-2101
- 11-digit product format
- 636292101
- Labeler code
- 63629
- Product ID
- 63629-2101_c002e436-b2c2-4eb7-87cd-3dbd7a9b91e0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Venlafaxine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA209193
- Marketing category
- ANDA
- Marketing start
- 2019-12-26
- Marketing end
- 0000-00-00
- Substance
- VENLAFAXINE HYDROCHLORIDE
- Active strength
- 225 mg/1
- Pharmacologic classes
- Norepinephrine Uptake Inhibitors [MoA], Serotonin Uptake Inhibitors [MoA], Serotonin and Norepinephrine Reuptake Inhibitor [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 63629-2101-1 | 63629210101 | 30 TABLET in 1 BOTTLE (63629-2101-1) | 30 tablet | 2019-12-26 | 0000-00-00 | No | No | Current |