Venlafaxine
- Product NDC
- 60760-159
- 11-digit product format
- 607600159
- Labeler code
- 60760
- Product ID
- 60760-159_7b3070fc-ce91-0d16-e053-2991aa0aa7cc
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Venlafaxine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- St. Mary's Medical Park Pharmacy
- Application
- ANDA202036
- Marketing category
- ANDA
- Marketing start
- 2016-04-19
- 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
- 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 |
|---|
| 60760-159-30 | 60760015930 | 30 TABLET in 1 BOTTLE, PLASTIC (60760-159-30) | 30 tablet | 2016-04-19 | 0000-00-00 | No | No | Current |