Trazodone Hydrochloride
- Product NDC
- 42291-835
- 11-digit product format
- 422910835
- Labeler code
- 42291
- Product ID
- 42291-835_c3df170e-8b75-5a43-e053-2995a90a71ff
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Trazodone Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- AvKARE
- Application
- ANDA071525
- Marketing category
- ANDA
- Marketing start
- 2014-02-06
- 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 42291-835-50 | 42291083550 | 500 TABLET in 1 BOTTLE (42291-835-50) | 500 tablet | 2014-02-06 | 0000-00-00 | No | No | Current |
| 42291-835-90 | 42291083590 | 90 TABLET in 1 BOTTLE (42291-835-90) | 90 tablet | 2016-06-27 | 0000-00-00 | No | No | Current |