Trazodone Hydrochloride
- Product NDC
- 58118-0429
- 11-digit product format
- 581180429
- Labeler code
- 58118
- Product ID
- 58118-0429_b026a386-5e37-52ed-e053-2a95a90a6b0e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Trazodone Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Clinical Solutions Wholesale, LLC
- Application
- ANDA071523
- Marketing category
- ANDA
- Marketing start
- 1990-09-30
- Marketing end
- 0000-00-00
- Substance
- TRAZODONE HYDROCHLORIDE
- Active strength
- 50 mg/1
- Pharmacologic classes
- Serotonin Reuptake Inhibitor [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 58118-0429-8 | 58118042908 | 30 TABLET in 1 BLISTER PACK (58118-0429-8) | 30 tablet | 2016-06-24 | 0000-00-00 | No | No | Current |