Venlafaxine Hydrochloride
- Product NDC
- 70518-2933
- 11-digit product format
- 705182933
- Labeler code
- 70518
- Product ID
- 70518-2933_dd16a908-4fdb-fd84-e053-2995a90a859f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Venlafaxine Hydrochloride
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA091272
- Marketing category
- ANDA
- Marketing start
- 2020-11-04
- 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 |
|---|
| 70518-2933-0 | 70518293300 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-2933-0) | 2020-11-04 | 0000-00-00 | No | No | Current |