Trazodone Hydrochloride
- Product NDC
- 68788-7004
- 11-digit product format
- 687887004
- Labeler code
- 68788
- Product ID
- 68788-7004_60a035e8-6b76-41d4-b170-51ed4a69d48f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Trazodone Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA071196
- Marketing category
- ANDA
- Marketing start
- 2017-08-11
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record