Trazodone Hydrochloride
- Product NDC
- 42291-833
- 11-digit product format
- 422910833
- Labeler code
- 42291
- Product ID
- 42291-833_de1d7168-0361-2ea8-e053-2995a90a2e8a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Trazodone Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- AvKARE
- Application
- ANDA071523
- Marketing category
- ANDA
- Marketing start
- 2014-02-06
- Marketing end
- 2022-06-30
- Substance
- TRAZODONE HYDROCHLORIDE
- Active strength
- 50 mg/1
- Pharmacologic classes
- Serotonin Reuptake Inhibitor [EPC]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- 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 |
|---|
| 42291-833-10 | 42291083310 | 1000 TABLET in 1 BOTTLE (42291-833-10) | 1000 tablet | 2014-02-06 | 0000-00-00 | No | No | Current |
| 42291-833-90 | 42291083390 | 90 TABLET in 1 BOTTLE (42291-833-90) | 90 tablet | 2016-06-27 | 0000-00-00 | No | No | Current |