Trazodone Hydrochloride
- Product NDC
- 71205-815
- 11-digit product format
- 712050815
- Labeler code
- 71205
- Product ID
- 71205-815_3c8c3d2b-9108-40fa-90d9-6ed545cf6549
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Trazodone Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA202180
- Marketing category
- ANDA
- Marketing start
- 2013-11-27
- Substance
- TRAZODONE HYDROCHLORIDE
- Active strength
- 150 mg/1
- Pharmacologic classes
- Serotonin Reuptake Inhibitor [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
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 | Sample | Exclude flag | Status |
|---|
| 71205-815-30 | 71205081530 | 30 TABLET in 1 BOTTLE (71205-815-30) | 30 tablet | 2023-06-19 | No | No | Historical |
| 71205-815-60 | 71205081560 | 60 TABLET in 1 BOTTLE (71205-815-60) | 60 tablet | 2023-06-19 | No | No | Historical |
| 71205-815-90 | 71205081590 | 90 TABLET in 1 BOTTLE (71205-815-90) | 90 tablet | 2023-06-19 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Trazodone Hydrochloride | Proficient Rx LP | 2023-06-01 | HUMAN PRESCRIPTION DRUG LABEL | 1 |