Trazodone Hydrochloride
- Product NDC
- 70518-1489
- 11-digit product format
- 705181489
- Labeler code
- 70518
- Product ID
- 70518-1489_c2c44c50-0a63-4072-e053-2995a90a882e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Trazodone Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA071524
- Marketing category
- ANDA
- Marketing start
- 2018-10-06
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-1489-0 | 70518148900 | 30 TABLET in 1 BLISTER PACK (70518-1489-0) | 30 tablet | 2018-10-06 | 0000-00-00 | No | No | Current |
| 70518-1489-1 | 70518148901 | 90 TABLET in 1 BOTTLE, PLASTIC (70518-1489-1) | 90 tablet | 2019-02-14 | 0000-00-00 | No | No | Current |