Paroxetine
- Product NDC
- 63629-8114
- 11-digit product format
- 636298114
- Labeler code
- 63629
- Product ID
- 63629-8114_987b9e46-981a-4c3e-9ff2-abeb9e3b4d35
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Paroxetine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA077584
- Marketing category
- ANDA
- Marketing start
- 2007-04-13
- Marketing end
- 0000-00-00
- Substance
- PAROXETINE HYDROCHLORIDE ANHYDROUS
- Active strength
- 20 mg/1
- Pharmacologic classes
- Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-8114-1 | 63629811401 | 90 TABLET, FILM COATED in 1 BOTTLE (63629-8114-1) | 2019-07-25 | 0000-00-00 | No | No | Current |
| 63629-8114-2 | 63629811402 | 30 TABLET, FILM COATED in 1 BOTTLE (63629-8114-2) | 2019-07-25 | 0000-00-00 | No | No | Current |