Trazodone Hydrochloride
- Product NDC
- 71335-0742
- 11-digit product format
- 713350742
- Labeler code
- 71335
- Product ID
- 71335-0742_337bd3ea-ccd3-7ae8-e063-6394a90a9b8f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Trazodone Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA205253
- Marketing category
- ANDA
- Marketing start
- 2017-12-11
- 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 |
|---|
| 71335-0742-1 | 71335074201 | 30 TABLET in 1 BOTTLE (71335-0742-1) | 30 tablet | 2022-02-09 | No | No | Historical |
| 71335-0742-2 | 71335074202 | 60 TABLET in 1 BOTTLE (71335-0742-2) | 60 tablet | 2022-02-09 | No | No | Historical |
| 71335-0742-3 | 71335074203 | 90 TABLET in 1 BOTTLE (71335-0742-3) | 90 tablet | 2022-02-09 | No | No | Historical |
| 71335-0742-4 | 71335074204 | 18 TABLET in 1 BOTTLE (71335-0742-4) | 18 tablet | 2022-02-09 | No | No | Historical |
| 71335-0742-5 | 71335074205 | 100 TABLET in 1 BOTTLE (71335-0742-5) | 100 tablet | 2022-02-09 | No | No | Historical |
| 71335-0742-6 | 71335074206 | 45 TABLET in 1 BOTTLE (71335-0742-6) | 45 tablet | 2022-02-09 | No | No | Historical |
| 71335-0742-7 | 71335074207 | 180 TABLET in 1 BOTTLE (71335-0742-7) | 180 tablet | 2022-02-09 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Trazodone Hydrochloride | Bryant Ranch Prepack | 2025-04-23 | HUMAN PRESCRIPTION DRUG LABEL | 103 |