Venlafaxine
- Product NDC
- 60760-186
- 11-digit product format
- 607600186
- Labeler code
- 60760
- Product ID
- 60760-186_7b306ae0-d071-b262-e053-2a91aa0a8b04
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Venlafaxine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- St. Mary
- Application
- ANDA202036
- Marketing category
- ANDA
- Marketing start
- 2017-12-26
- Marketing end
- 0000-00-00
- Substance
- VENLAFAXINE HYDROCHLORIDE
- Active strength
- 38 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 |
|---|
| 60760-186-60 | 60760018660 | 60 TABLET in 1 BOTTLE, PLASTIC (60760-186-60) | 60 tablet | 2017-12-26 | 0000-00-00 | No | No | Current |