PAXIL
- Product NDC
- 70518-2636
- 11-digit product format
- 705182636
- Labeler code
- 70518
- Product ID
- 70518-2636_cc0932f2-f36f-6820-e053-2a95a90a40aa
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- paroxetine hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- NDA020031
- Marketing category
- NDA
- Marketing start
- 2020-03-18
- Marketing end
- 0000-00-00
- Substance
- PAROXETINE HYDROCHLORIDE HEMIHYDRATE
- Active strength
- 10 mg/1
- Pharmacologic classes
- Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]
- 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-2636-0 | 70518263600 | 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-2636-0) | 2020-03-18 | 0000-00-00 | No | No | Current |