Trazodone Hydrochloride
- Product NDC
- 71205-574
- 11-digit product format
- 712050574
- Labeler code
- 71205
- Product ID
- 71205-574_82b1165a-6f2c-470c-adff-9db816fb0ad4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Trazodone Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA071524
- Marketing category
- ANDA
- Marketing start
- 2020-10-08
- Substance
- TRAZODONE HYDROCHLORIDE
- Active strength
- 100 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 |
|---|
| 71205-574-30 | 71205057430 | 30 TABLET in 1 BOTTLE (71205-574-30) | 30 tablet | 2021-06-08 | No | No | Historical |
| 71205-574-60 | 71205057460 | 60 TABLET in 1 BOTTLE (71205-574-60) | 60 tablet | 2021-06-08 | No | No | Historical |
| 71205-574-90 | 71205057490 | 90 TABLET in 1 BOTTLE (71205-574-90) | 90 tablet | 2021-06-08 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Trazodone Hydrochloride | Proficient Rx LP | 2023-05-01 | HUMAN PRESCRIPTION DRUG LABEL | 2 |