venlafaxine hydrochloride
- Product NDC
- 50090-5930
- 11-digit product format
- 500905930
- Labeler code
- 50090
- Product ID
- 50090-5930_a1b8e563-a468-40e6-b752-2529d512a026
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- venlafaxine hydrochloride
- Dosage form
- CAPSULE, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA090174
- Marketing category
- ANDA
- Marketing start
- 2021-06-10
- Marketing end
- 0000-00-00
- Substance
- VENLAFAXINE HYDROCHLORIDE
- Active strength
- 38 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 |
|---|
| 50090-5930-0 | 50090593000 | 33 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (50090-5930-0) | 2022-03-02 | 0000-00-00 | No | No | Current |