Venlafaxine Hydrochloride
- Product NDC
- 55154-3362
- 11-digit product format
- 551543362
- Labeler code
- 55154
- Product ID
- 55154-3362_6bd781d6-deca-4e28-a168-d83c8b8fe205
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Venlafaxine Hydrochloride
- Dosage form
- CAPSULE, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Cardinal Health 107, LLC
- Application
- ANDA090899
- Marketing category
- ANDA
- Marketing start
- 2015-04-06
- Marketing end
- 2023-06-30
- 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
- 0000-00-00
- 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 |
|---|
| 55154-3362-0 | 55154336200 | 10 BLISTER PACK in 1 BAG (55154-3362-0) > 1 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK | 10 blister pack | 2015-04-06 | 2023-06-30 | No | No | Current |