Trazodone Hydrochloride
- Product NDC
- 50090-4402
- 11-digit product format
- 500904402
- Labeler code
- 50090
- Product ID
- 50090-4402_43c75a41-5d8a-4730-9427-82f8f8b49b84
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Trazodone Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- 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 |
|---|
| 50090-4402-0 | 50090440200 | 33 BLISTER PACK in 1 CARTON (50090-4402-0) > 1 TABLET in 1 BLISTER PACK | 33 blister pack | 2019-06-28 | 0000-00-00 | No | No | Current |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Trazodone Hydrochloride | A-S Medication Solutions | 2019-07-26 | HUMAN PRESCRIPTION DRUG LABEL | 2 |