Trazodone Hydrochloride
- Product NDC
- 70934-620
- 11-digit product format
- 709340620
- Labeler code
- 70934
- Product ID
- 70934-620_ab6d77d7-0a95-739d-e053-2995a90afff0
- 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
- 2020-03-23
- 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
- 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 |
|---|
| 70934-620-30 | 70934062030 | 30 TABLET in 1 BOTTLE, PLASTIC (70934-620-30) | 30 tablet | 2020-03-23 | 0000-00-00 | No | No | Current |
| 70934-620-90 | 70934062090 | 90 TABLET in 1 BOTTLE, PLASTIC (70934-620-90) | 90 tablet | 2020-04-24 | 0000-00-00 | No | No | Current |