Venlafaxine hydrochloride
- Product NDC
- 50090-5732
- 11-digit product format
- 500905732
- Labeler code
- 50090
- Product ID
- 50090-5732_0fb60983-07ab-4ce5-9047-9089ad2c7d46
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Venlafaxine hydrochloride
- Dosage form
- CAPSULE, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA204889
- Marketing category
- ANDA
- Marketing start
- 2017-10-06
- 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 |
|---|
| 50090-5732-0 | 50090573200 | 29 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (50090-5732-0) | 2021-09-28 | 0000-00-00 | No | No | Current |