Trazodone Hydrochloride
- Product NDC
- 63629-7287
- 11-digit product format
- 636297287
- Labeler code
- 63629
- Product ID
- 63629-7287_10a30879-f6e2-4030-95b8-0979c18c418a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Trazodone Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA071196
- Marketing category
- ANDA
- Marketing start
- 1999-05-03
- Marketing end
- 2022-10-31
- Substance
- TRAZODONE HYDROCHLORIDE
- Active strength
- 300 mg/1
- Pharmacologic classes
- Serotonin Reuptake Inhibitor [EPC]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- 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 |
|---|
| 63629-7287-1 | 63629728701 | 60 TABLET in 1 BOTTLE (63629-7287-1) | 60 tablet | 2017-05-25 | 0000-00-00 | No | No | Current |
| 63629-7287-2 | 63629728702 | 30 TABLET in 1 BOTTLE (63629-7287-2) | 30 tablet | 2017-05-25 | 0000-00-00 | No | No | Current |
| 63629-7287-3 | 63629728703 | 18 TABLET in 1 BOTTLE (63629-7287-3) | 18 tablet | 2017-05-25 | 0000-00-00 | No | No | Current |