Trazodone Hydrochloride
- Product NDC
- 70518-1441
- 11-digit product format
- 705181441
- Labeler code
- 70518
- Product ID
- 70518-1441_c2aefc39-55a9-50d3-e053-2995a90a2158
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Trazodone Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA071525
- Marketing category
- ANDA
- Marketing start
- 2018-09-27
- 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
- 2022-12-31
- 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 |
|---|
| 70518-1441-0 | 70518144100 | 30 TABLET in 1 BLISTER PACK (70518-1441-0) | 30 tablet | 2018-09-27 | 0000-00-00 | No | No | Current |
| 70518-1441-1 | 70518144101 | 90 TABLET in 1 BOTTLE, PLASTIC (70518-1441-1) | 90 tablet | 2019-01-28 | 0000-00-00 | No | No | Current |