Venlafaxine Hydrochloride
- Product NDC
- 52343-131
- 11-digit product format
- 523430131
- Labeler code
- 52343
- Product ID
- 52343-131_a34da1e9-5c34-400c-8371-6ca54c1580f9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Venlafaxine Hydrochloride
- Dosage form
- CAPSULE, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- ACETRIS HEALTH, LLC
- Application
- ANDA200834
- Marketing category
- ANDA
- Marketing start
- 2011-06-01
- Marketing end
- 0000-00-00
- Substance
- VENLAFAXINE HYDROCHLORIDE
- Active strength
- 38 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 |
|---|
| 52343-131-30 | 52343013130 | 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (52343-131-30) | 2011-06-01 | 0000-00-00 | No | No | Current |
| 52343-131-90 | 52343013190 | 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (52343-131-90) | 2011-06-01 | 0000-00-00 | No | No | Current |