Desvenlafaxine
- Product NDC
- 68382-741
- 11-digit product format
- 683820741
- Labeler code
- 68382
- Product ID
- 68382-741_281d1f1b-df9d-4c11-86c3-df47e59fe8b0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Desvenlafaxine
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Zydus Pharmaceuticals USA Inc.
- Application
- ANDA204020
- Marketing category
- ANDA
- Marketing start
- 2018-05-08
- Marketing end
- 0000-00-00
- Substance
- DESVENLAFAXINE
- Active strength
- 100 mg/1
- Pharmacologic classes
- Cytochrome P450 2D6 Inhibitors [MoA], Norepinephrine Uptake Inhibitors [MoA], Serotonin Uptake Inhibitors [MoA], Serotonin and Norepinephrine Reuptake Inhibitor [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2024-12-31
- 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 |
|---|
| 68382-741-01 | 68382074101 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-741-01) | | 2018-05-08 | 0000-00-00 | No | No | Current |
| 68382-741-05 | 68382074105 | 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-741-05) | | 2018-05-08 | 0000-00-00 | No | No | Current |
| 68382-741-06 | 68382074106 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-741-06) | | 2018-05-08 | 0000-00-00 | No | No | Current |
| 68382-741-10 | 68382074110 | 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-741-10) | | 2018-05-08 | 0000-00-00 | No | No | Current |
| 68382-741-16 | 68382074116 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-741-16) | | 2018-05-08 | 0000-00-00 | No | No | Current |
| 68382-741-67 | 68382074167 | 14 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-741-67) | | 2018-05-08 | 0000-00-00 | No | No | Current |
| 68382-741-77 | 68382074177 | 10 BLISTER PACK in 1 CARTON (68382-741-77) > 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (68382-741-30) | 10 blister pack | 2018-05-08 | 0000-00-00 | No | No | Current |