Trazodone Hydrochloride
- Product NDC
- 70771-1938
- 11-digit product format
- 707711938
- Labeler code
- 70771
- Product ID
- 70771-1938_0b9d3b91-26ed-477b-a88e-2d6a76fedabf
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Trazodone Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Zydus Lifesciences Limited
- Application
- ANDA205253
- Marketing category
- ANDA
- Marketing start
- 2026-01-22
- Substance
- TRAZODONE HYDROCHLORIDE
- Active strength
- 50 mg/1
- Pharmacologic classes
- Serotonin Reuptake Inhibitor [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- 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 |
|---|
| 70771-1938-0 | 70771193800 | 1000 TABLET in 1 BOTTLE (70771-1938-0) | 1000 tablet | 2026-01-22 | No | No | Historical |
| 70771-1938-1 | 70771193801 | 100 TABLET in 1 BOTTLE (70771-1938-1) | 100 tablet | 2026-01-22 | No | No | Historical |
| 70771-1938-5 | 70771193805 | 500 TABLET in 1 BOTTLE (70771-1938-5) | 500 tablet | 2026-01-22 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| TRAZODONE HYDROCHLORIDE TABLETS | Zydus Lifesciences Limited | Zydus Pharmaceuticals Limited | 2026-01-23 | HUMAN PRESCRIPTION DRUG LABEL | 8 |