TRAZODONE HYDROCHLORIDE
- Product NDC
- 61919-912
- 11-digit product format
- 619190912
- Labeler code
- 61919
- Product ID
- 61919-912_874609ee-c815-42a0-e053-2995a90a5e4b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- TRAZODONE HYDROCHLORIDE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- DIRECT RX
- Application
- ANDA071523
- Marketing category
- ANDA
- Marketing start
- 2017-11-01
- Marketing end
- 0000-00-00
- Substance
- TRAZODONE HYDROCHLORIDE
- Active strength
- 300 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