Trazodone Hydrochloride
- Product NDC
- 68788-9341
- 11-digit product format
- 687889341
- Labeler code
- 68788
- Product ID
- 68788-9341_38adc471-393b-46c3-811d-279dcb80df97
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Trazodone Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals
- Application
- ANDA071525
- Marketing category
- ANDA
- Marketing start
- 2016-06-15
- Marketing end
- 0000-00-00
- Substance
- TRAZODONE HYDRO
- Active strength
- 150 mg/1
- Pharmacologic classes
- Serotonin Reupt
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- Current FDA listing
- Historical FDA.report record