Trazodone Hydrochloride
- Product NDC
- 63629-8140
- 11-digit product format
- 636298140
- Labeler code
- 63629
- Product ID
- 63629-8140_c50082d3-88cc-4be3-97b2-51629609aaf2
- 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
- Marketing end
- 0000-00-00
- Substance
- TRAZODONE HYDROCHLORIDE
- Active strength
- 50 mg/1
- Pharmacologic classes
- Serotonin Reuptake Inhibitor [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
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 | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-8140-1 | 63629814001 | 30 TABLET in 1 BOTTLE (63629-8140-1) | 30 tablet | 2019-08-26 | 0000-00-00 | No | No | Current |