Venlafaxine HCL
- Product NDC
- 80425-0088
- 11-digit product format
- 804250088
- Labeler code
- 80425
- Product ID
- 80425-0088_edaf13e8-06dd-3a8b-e053-2a95a90ad808
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Venlafaxine HCL
- Dosage form
- CAPSULE, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Advanced Rx Pharmacy of Tennessee, 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 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 |
|---|
| 80425-0088-2 | 80425008802 | 60 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (80425-0088-2) | 2011-01-06 | 0000-00-00 | No | No | Current |