Trazodone Hydrochloride
- Product NDC
- 0555-0733
- 11-digit product format
- 005550733
- Labeler code
- 0555
- Product ID
- 0555-0733_36d1861c-f184-416d-b708-77d15f1c8dcb
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Trazodone Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Teva Pharmaceuticals USA, Inc.
- 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 |
|---|
| 0555-0733-02 | 00555073302 | 100 TABLET in 1 BOTTLE (0555-0733-02) | 100 tablet | 1999-05-03 | 2022-10-31 | No | No | Current |