Trazodone Hydrochloride
- Product NDC
- 50090-2759
- 11-digit product format
- 500902759
- Labeler code
- 50090
- Product ID
- 50090-2759_18a84edc-8954-47e7-8cdf-e57afd7315e7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Trazodone Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA071196
- Marketing category
- ANDA
- Marketing start
- 2008-11-17
- Marketing end
- 0000-00-00
- Substance
- TRAZODONE HYDROCHLORIDE
- Active strength
- 100 mg/1
- Pharmacologic classes
- Serotonin Reuptake Inhibitor [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- 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 |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Trazodone Hydrochloride | A-S Medication Solutions | 2018-06-29 | HUMAN PRESCRIPTION DRUG LABEL | 9 |