VENLAFAXINE HYDROCHLORIDE
- Product NDC
- 13668-020
- 11-digit product format
- 136680020
- Labeler code
- 13668
- Product ID
- 13668-020_ebf43b7f-1550-6b6a-e053-2995a90a3fef
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- VENLAFAXINE HYDROCHLORIDE
- Dosage form
- CAPSULE, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Torrent Pharmaceuticals Limited
- Application
- ANDA090899
- Marketing category
- ANDA
- Marketing start
- 2011-01-06
- Marketing end
- 0000-00-00
- Substance
- VENLAFAXINE HYDROCHLORIDE
- Active strength
- 150 mg/1
- Pharmacologic classes
- Norepinephrine Uptake Inhibitors [MoA], Serotonin Uptake Inhibitors [MoA], Serotonin and Norepinephrine Reuptake Inhibitor [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 13668-020-01 | 13668002001 | 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (13668-020-01) | 2011-01-06 | 0000-00-00 | No | No | Current |
| 13668-020-05 | 13668002005 | 500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (13668-020-05) | 2011-01-06 | 0000-00-00 | No | No | Current |
| 13668-020-30 | 13668002030 | 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (13668-020-30) | 2011-01-06 | 0000-00-00 | No | No | Current |
| 13668-020-74 | 13668002074 | 100 CAPSULE, EXTENDED RELEASE in 1 CARTON (13668-020-74) | 2011-01-06 | 0000-00-00 | No | No | Current |
| 13668-020-90 | 13668002090 | 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (13668-020-90) | 2011-01-06 | 0000-00-00 | No | No | Current |