Venlafaxine Hydrochloride
- Product NDC
- 71335-0563
- 11-digit product format
- 713350563
- Labeler code
- 71335
- Product ID
- 71335-0563_a655d04e-645d-4d85-a6d7-f84665bfa25b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Venlafaxine Hydrochloride
- Dosage form
- CAPSULE, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA076565
- Marketing category
- ANDA
- Marketing start
- 2010-07-01
- Marketing end
- 0000-00-00
- Substance
- VENLAFAXINE HYDROCHLORIDE
- Active strength
- 75 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71335-0563-1 | 71335056301 | 60 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71335-0563-1) | 2011-03-24 | 0000-00-00 | No | No | Current |
| 71335-0563-2 | 71335056302 | 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71335-0563-2) | 2011-03-24 | 0000-00-00 | No | No | Current |
| 71335-0563-3 | 71335056303 | 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71335-0563-3) | 2011-03-24 | 0000-00-00 | No | No | Current |
| 71335-0563-4 | 71335056304 | 28 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71335-0563-4) | 2011-03-24 | 0000-00-00 | No | No | Current |
| 71335-0563-5 | 71335056305 | 120 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71335-0563-5) | 2011-03-24 | 0000-00-00 | No | No | Current |
| 71335-0563-6 | 71335056306 | 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71335-0563-6) | 2011-03-24 | 0000-00-00 | No | No | Current |