Trazodone Hydrochloride
- Product NDC
- 71335-0164
- 11-digit product format
- 713350164
- Labeler code
- 71335
- Product ID
- 71335-0164_ebafe312-212f-45bb-842c-c9712fe06e0f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Trazodone Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA071196
- Marketing category
- ANDA
- Marketing start
- 2008-11-17
- Marketing end
- 0000-00-00
- Substance
- TRAZODONE HYDROCHLORIDE
- Active strength
- 150 mg/1
- Pharmacologic classes
- Serotonin Reuptake Inhibitor [EPC]
- 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 |
|---|
| 71335-0164-1 | 71335016401 | 30 TABLET in 1 BOTTLE (71335-0164-1) | 30 tablet | 2017-03-24 | 0000-00-00 | No | No | Current |
| 71335-0164-2 | 71335016402 | 60 TABLET in 1 BOTTLE (71335-0164-2) | 60 tablet | 2017-03-24 | 0000-00-00 | No | No | Current |
| 71335-0164-3 | 71335016403 | 90 TABLET in 1 BOTTLE (71335-0164-3) | 90 tablet | 2017-03-24 | 0000-00-00 | No | No | Current |
| 71335-0164-4 | 71335016404 | 18 TABLET in 1 BOTTLE (71335-0164-4) | 18 tablet | 2017-03-24 | 0000-00-00 | No | No | Current |