Trazodone Hydrochloride
- Product NDC
- 50090-2374
- 11-digit product format
- 500902374
- Labeler code
- 50090
- Product ID
- 50090-2374_c038b3e0-7864-4a56-896f-a5b2d7e6c0ea
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Trazodone Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA071196
- Marketing category
- ANDA
- Marketing start
- 2008-11-17
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-2374-1 | 50090237401 | 6 TABLET in 1 BOTTLE (50090-2374-1) | 6 tablet | 2019-02-04 | 0000-00-00 | No | No | Current |
| 50090-2374-2 | 50090237402 | 30 TABLET in 1 BOTTLE (50090-2374-2) | 30 tablet | 2016-04-26 | 0000-00-00 | No | No | Current |
| 50090-2374-4 | 50090237404 | 90 TABLET in 1 BOTTLE (50090-2374-4) | 90 tablet | 2018-04-24 | 0000-00-00 | No | No | Current |