VENLAFAXINE HYDROCHLORIDE
- Product NDC
- 55700-518
- 11-digit product format
- 557000518
- Labeler code
- 55700
- Product ID
- 55700-518_8d55ce19-ab14-42e8-bf83-14ed887c4705
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- VENLAFAXINE HYDROCHLORIDE
- Dosage form
- CAPSULE, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Lake Erie Medical DBA Quality Care Products LLC
- Application
- ANDA090899
- Marketing category
- ANDA
- Marketing start
- 2011-01-06
- 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 |
|---|
| 55700-518-30 | 55700051830 | 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (55700-518-30) | 2017-04-21 | 0000-00-00 | No | No | Current |
| 55700-518-60 | 55700051860 | 60 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (55700-518-60) | 2018-07-20 | 0000-00-00 | No | No | Current |