Nefazodone Hydrochloride
- Product NDC
- 68788-7246
- 11-digit product format
- 687887246
- Labeler code
- 68788
- Product ID
- 68788-7246_5db7a326-323c-4519-b040-a8fdbe106685
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Nefazodone Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA076037
- Marketing category
- ANDA
- Marketing start
- 2018-08-20
- Marketing end
- 0000-00-00
- Substance
- NEFAZODONE HYDROCHLORIDE
- Active strength
- 150 mg/1
- Pharmacologic classes
- Serotonin Reuptake Inhibitor [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 68788-7246-1 | 68788724601 | 100 TABLET in 1 BOTTLE (68788-7246-1) | 100 tablet | 2018-08-20 | 0000-00-00 | No | No | Current |
| 68788-7246-3 | 68788724603 | 30 TABLET in 1 BOTTLE (68788-7246-3) | 30 tablet | 2018-08-20 | 0000-00-00 | No | No | Current |
| 68788-7246-6 | 68788724606 | 60 TABLET in 1 BOTTLE (68788-7246-6) | 60 tablet | 2018-08-20 | 0000-00-00 | No | No | Current |
| 68788-7246-8 | 68788724608 | 120 TABLET in 1 BOTTLE (68788-7246-8) | 120 tablet | 2018-08-20 | 0000-00-00 | No | No | Current |
| 68788-7246-9 | 68788724609 | 90 TABLET in 1 BOTTLE (68788-7246-9) | 90 tablet | 2018-08-20 | 0000-00-00 | No | No | Current |