Nefazodone Hydrochloride
- Product NDC
- 63629-7214
- 11-digit product format
- 636297214
- Labeler code
- 63629
- Product ID
- 63629-7214_498ea1ce-c77a-4a4d-9d1f-ea7bd58a92a9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Nefazodone Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA076037
- Marketing category
- ANDA
- Marketing start
- 2003-09-16
- Marketing end
- 0000-00-00
- Substance
- NEFAZODONE HYDROCHLORIDE
- Active strength
- 250 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
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-7214-1 | 63629721401 | 60 TABLET in 1 BOTTLE (63629-7214-1) | 60 tablet | 2017-03-16 | 0000-00-00 | No | No | Current |
| 63629-7214-2 | 63629721402 | 30 TABLET in 1 BOTTLE (63629-7214-2) | 30 tablet | 2017-03-16 | 0000-00-00 | No | No | Current |