Trazodone Hydrochloride
- Product NDC
- 55700-921
- 11-digit product format
- 557000921
- Labeler code
- 55700
- Product ID
- 55700-921_06e47a54-1a8b-4a70-82d3-47fed02d18a3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Trazodone Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Quality Care Products, LLC
- Application
- ANDA205253
- Marketing category
- ANDA
- Marketing start
- 2021-08-24
- 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 |
|---|
| 55700-921-30 | 55700092130 | 30 TABLET in 1 BOTTLE (55700-921-30) | 30 tablet | 2021-08-24 | 0000-00-00 | No | No | Current |
| 55700-921-90 | 55700092190 | 90 TABLET in 1 BOTTLE (55700-921-90) | 90 tablet | 2022-02-18 | 0000-00-00 | No | No | Current |