venlafaxine
- Product NDC
- 70934-761
- 11-digit product format
- 709340761
- Labeler code
- 70934
- Product ID
- 70934-761_a9c6238c-52d5-529d-e053-2995a90aa0cd
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- venlafaxine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Denton Pharma, Inc. DBA Northwind Pharmaceuticals
- Application
- ANDA078932
- Marketing category
- ANDA
- Marketing start
- 2020-05-29
- Marketing end
- 0000-00-00
- Substance
- VENLAFAXINE HYDROCHLORIDE
- Active strength
- 75 mg/1
- Pharmacologic classes
- Norepinephrine Uptake Inhibitors [MoA],Serotonin and Norepinephrine Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70934-761-90 | 70934076190 | 90 TABLET in 1 BOTTLE, PLASTIC (70934-761-90) | 90 tablet | 2020-05-29 | 0000-00-00 | No | No | Current |