Trazodone Hydrochloride
- Product NDC
- 70518-1195
- 11-digit product format
- 705181195
- Labeler code
- 70518
- Product ID
- 70518-1195_909b60ff-4b6b-1eeb-e053-2995a90ae73d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Trazodone Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA071196
- Marketing category
- ANDA
- Marketing start
- 2018-05-14
- Marketing end
- 0000-00-00
- Substance
- TRAZODONE HYDROCHLORIDE
- Active strength
- 150 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