Trazodone Hydrochloride
- Product NDC
- 60760-807
- 11-digit product format
- 607600807
- Labeler code
- 60760
- Product ID
- 60760-807_7b2ff573-ca0e-d69a-e053-2a91aa0abcec
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Trazodone Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- St. Mary's Medical Park Pharmacy
- Application
- ANDA205253
- Marketing category
- ANDA
- Marketing start
- 2018-03-06
- Marketing end
- 0000-00-00
- Substance
- TRAZODONE HYDROCHLORIDE
- Active strength
- 150 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 |
|---|
| 60760-807-30 | 60760080730 | 30 TABLET in 1 BOTTLE, PLASTIC (60760-807-30) | 30 tablet | 2018-03-06 | 0000-00-00 | No | No | Current |