Trazodone Hydrochloride
- Product NDC
- 55700-739
- 11-digit product format
- 557000739
- Labeler code
- 55700
- Product ID
- 55700-739_08b58cb8-b488-4156-a25e-760783530880
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Trazodone Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Quality Care Products, LLC
- Application
- ANDA206923
- Marketing category
- ANDA
- Marketing start
- 2019-04-05
- 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 |
|---|
| 55700-739-30 | 55700073930 | 30 TABLET in 1 BOTTLE (55700-739-30) | 30 tablet | 2019-04-05 | 0000-00-00 | No | No | Current |
| 55700-739-60 | 55700073960 | 60 TABLET in 1 BOTTLE (55700-739-60) | 60 tablet | 2019-04-05 | 0000-00-00 | No | No | Current |
| 55700-739-90 | 55700073990 | 90 TABLET in 1 BOTTLE (55700-739-90) | 90 tablet | 2021-12-03 | 0000-00-00 | No | No | Current |