Trazodone Hydrochloride
- Product NDC
- 70934-817
- 11-digit product format
- 709340817
- Labeler code
- 70934
- Product ID
- 70934-817_b9d0306b-7b23-6e6c-e053-2995a90a94fb
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Trazodone Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Denton Pharma, Inc. DBA Northwind Pharmaceuticals
- Application
- ANDA202180
- Marketing category
- ANDA
- Marketing start
- 2021-01-25
- Marketing end
- 0000-00-00
- Substance
- TRAZODONE HYDROCHLORIDE
- Active strength
- 100 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
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 |
|---|
| 70934-817-30 | 70934081730 | 30 TABLET in 1 BOTTLE, PLASTIC (70934-817-30) | 30 tablet | 2021-01-25 | 0000-00-00 | No | No | Current |
| 70934-817-90 | 70934081790 | 90 TABLET in 1 BOTTLE, PLASTIC (70934-817-90) | 90 tablet | 2021-01-25 | 0000-00-00 | No | No | Current |