venlafaxine
- Product NDC
- 16714-315
- 11-digit product format
- 167140315
- Labeler code
- 16714
- Product ID
- 16714-315_16f95a4f-2f1f-48c0-8501-c5dc2232a5d7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- venlafaxine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NorthStar RxLLC
- Application
- ANDA078932
- Marketing category
- ANDA
- Marketing start
- 2010-12-21
- Marketing end
- 0000-00-00
- Substance
- VENLAFAXINE HYDROCHLORIDE
- Active strength
- 100 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
- 2020-12-31
- 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 |
|---|
| 16714-315-01 | 16714031501 | 100 TABLET in 1 BOTTLE (16714-315-01) | 100 tablet | 2010-12-21 | 0000-00-00 | No | No | Current |
| 16714-315-02 | 16714031502 | 30 TABLET in 1 BOTTLE (16714-315-02) | 30 tablet | 2010-12-21 | 0000-00-00 | No | No | Current |
| 16714-315-03 | 16714031503 | 1000 TABLET in 1 BOTTLE (16714-315-03) | 1000 tablet | 2010-12-21 | 0000-00-00 | No | No | Current |