venlafaxine
- Product NDC
- 55700-816
- 11-digit product format
- 557000816
- Labeler code
- 55700
- Product ID
- 55700-816_09e50fc0-1bcc-4ef4-b57e-6d26c25ebcdd
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- venlafaxine hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Quality Care Products, LLC
- Application
- ANDA090555
- Marketing category
- ANDA
- Marketing start
- 2019-11-08
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 55700-816-90 | 55700081690 | 90 TABLET in 1 BOTTLE (55700-816-90) | 90 tablet | 2019-11-08 | 0000-00-00 | No | No | Current |