Trazodone Hydrochloride
- Product NDC
- 70934-370
- 11-digit product format
- 709340370
- Labeler code
- 70934
- Product ID
- 70934-370_af4aff31-516e-e316-e053-2a95a90a57eb
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Trazodone Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Denton Pharma, Inc. DBA Northwind Pharmaceuticals
- Application
- ANDA206923
- Marketing category
- ANDA
- Marketing start
- 2019-05-20
- 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
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 |
|---|
| 70934-370-30 | 70934037030 | 30 TABLET in 1 BOTTLE, PLASTIC (70934-370-30) | 30 tablet | 2019-05-20 | 0000-00-00 | No | No | Current |
| 70934-370-90 | 70934037090 | 90 TABLET in 1 BOTTLE, PLASTIC (70934-370-90) | 90 tablet | 2019-10-22 | 0000-00-00 | No | No | Current |