TRAZODONE HYDROCHLORIDE
- Product NDC
- 61919-613
- 11-digit product format
- 619190613
- Labeler code
- 61919
- Product ID
- 61919-613_e9d12528-11c0-b9ed-e053-2995a90af9ed
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- TRAZODONE HYDROCHLORIDE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Direct_Rx
- Application
- ANDA205253
- Marketing category
- ANDA
- Marketing start
- 2019-08-19
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 6E8ZO8LRNM | TRAZODONE HYDROCHLORIDE | 25332-39-2 | TRAZODONE HYDROCHLORIDE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 61919-613-30 | 61919061330 | 30 TABLET in 1 BOTTLE (61919-613-30) | 30 tablet | 2022-09-27 | 0000-00-00 | No | No | Current |
| 61919-613-60 | 61919061360 | 60 TABLET in 1 BOTTLE (61919-613-60) | 60 tablet | 2019-08-19 | 0000-00-00 | No | No | Current |
| 61919-613-90 | 61919061390 | 90 TABLET in 1 BOTTLE (61919-613-90) | 90 tablet | 2019-08-19 | 0000-00-00 | No | No | Current |