PAXIL
- Product NDC
- 71335-0572
- 11-digit product format
- 713350572
- Labeler code
- 71335
- Product ID
- 71335-0572_ba697f67-8406-4416-bdfa-e1b5ce6a9a68
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- paroxetine hydrochloride
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- NDA020936
- Marketing category
- NDA
- Marketing start
- 2011-01-01
- Marketing end
- 0000-00-00
- Substance
- PAROXETINE HYDROCHLORIDE ANHYDROUS
- Active strength
- 25 mg/1
- Pharmacologic classes
- Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]
- 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71335-0572-1 | 71335057201 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0572-1) | 2011-01-01 | 0000-00-00 | No | No | Current |
| 71335-0572-2 | 71335057202 | 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0572-2) | 2011-01-01 | 0000-00-00 | No | No | Current |