Venlafaxine
- Product NDC
- 16714-656
- 11-digit product format
- 167140656
- Labeler code
- 16714
- Product ID
- 16714-656_ee8cb936-5e51-e8a6-e053-2a95a90a4278
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Venlafaxine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Northstar Rx LLC
- Application
- ANDA078627
- Marketing category
- ANDA
- Marketing start
- 2017-01-26
- Marketing end
- 2024-09-30
- 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
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 16714-656-01 | 16714065601 | 100 TABLET in 1 BOTTLE (16714-656-01) | 100 tablet | 2017-01-26 | 0000-00-00 | No | No | Current |