Venlafaxine Hydrochloride
- Product NDC
- 50090-5892
- 11-digit product format
- 500905892
- Labeler code
- 50090
- Product ID
- 50090-5892_5015dce3-2f7e-4ef6-a1b5-43767e0b79f0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Venlafaxine Hydrochloride
- Dosage form
- CAPSULE, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA212277
- Marketing category
- ANDA
- Marketing start
- 2019-07-08
- 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 |
|---|
| 50090-5892-0 | 50090589200 | 29 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (50090-5892-0) | 2022-01-11 | 0000-00-00 | No | No | Current |