Trazodone Hydrochloride
- Product NDC
- 60760-434
- 11-digit product format
- 607600434
- Labeler code
- 60760
- Product ID
- 60760-434_7b2fcd4a-7be6-6fa8-e053-2991aa0a7909
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Trazodone Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- St. Mary's Medical Park Pharmacy
- Application
- ANDA072193
- 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
- 2019-12-31
- Current FDA listing
- Historical FDA.report record