TRAZODONE HYDROCHLORIDE
- Product NDC
- 72162-2533
- 11-digit product format
- 721622533
- Labeler code
- 72162
- Product ID
- 72162-2533_f3343d6f-0995-44bf-baba-c6446880e5e8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- TRAZODONE HYDROCHLORIDE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA204852
- Marketing category
- ANDA
- Marketing start
- 2015-09-15
- Substance
- TRAZODONE HYDROCHLORIDE
- Active strength
- 300 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 |
|---|
| 72162-2533-1 | 72162253301 | 100 TABLET in 1 BOTTLE (72162-2533-1) | 100 tablet | 2025-09-19 | No | No | Historical |
| 72162-2533-5 | 72162253305 | 500 TABLET in 1 BOTTLE (72162-2533-5) | 500 tablet | 2025-09-19 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| TRAZODONE HYDROCHLORIDE | Bryant Ranch Prepack | 2025-09-19 | HUMAN PRESCRIPTION DRUG LABEL | 101 |