Venlafaxine Hydrochloride
- Product NDC
- 60429-866
- 11-digit product format
- 604290866
- Labeler code
- 60429
- Product ID
- 60429-866_a024d3b3-3bf6-1517-e053-2995a90a4acb
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- venlafaxine hydrochloride
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Golden State Medical Supply
- Application
- ANDA205468
- Marketing category
- ANDA
- Marketing start
- 2017-03-24
- Marketing end
- 0000-00-00
- Substance
- VENLAFAXINE HYDROCHLORIDE
- Active strength
- 150 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 60429-866-30 | 60429086630 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (60429-866-30) | 2017-04-05 | 0000-00-00 | No | No | Current |
| 60429-866-90 | 60429086690 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (60429-866-90) | 2017-04-05 | 0000-00-00 | No | No | Current |