TRAZODONE HYDROCHLORIDE
- Product NDC
- 61919-231
- 11-digit product format
- 619190231
- Labeler code
- 61919
- Product ID
- 61919-231_94f405d3-4f65-5405-e053-2995a90a9bd1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- TRAZODONE HYDROCHLORIDE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Direct_Rx
- Application
- ANDA071523
- Marketing category
- ANDA
- Marketing start
- 2014-01-01
- Marketing end
- 0000-00-00
- Substance
- TRAZODONE HYDROCHLORIDE
- Active strength
- 50 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 |
|---|
| 61919-231-30 | 61919023130 | 30 TABLET in 1 BOTTLE (61919-231-30) | 30 tablet | 2019-09-18 | 0000-00-00 | No | No | Current |
| 61919-231-60 | 61919023160 | 60 TABLET in 1 BOTTLE (61919-231-60) | 60 tablet | 2019-09-18 | 0000-00-00 | No | No | Current |
| 61919-231-82 | 61919023182 | 180 TABLET in 1 BOTTLE (61919-231-82) | 180 tablet | 2014-01-01 | 0000-00-00 | No | No | Current |
| 61919-231-90 | 61919023190 | 90 TABLET in 1 BOTTLE (61919-231-90) | 90 tablet | 2019-09-18 | 0000-00-00 | No | No | Current |