Trazodone Hydrochloride
- Product NDC
- 66267-392
- 11-digit product format
- 662670392
- Labeler code
- 66267
- Product ID
- 66267-392_9cbd33ff-eec7-488d-e053-2a95a90a9202
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Trazodone Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals, Inc.
- Application
- ANDA072192
- Marketing category
- ANDA
- Marketing start
- 2010-05-30
- 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
- 2021-12-31
- Current FDA listing
- Historical FDA.report record