NDC 69584-672 – Paroxetine hydrochloride
Paroxetine Hydrochloride 20 mg/1 · Tablet, Film Coated · Oral
Product NDC69584-672
Product details
- Brand name
- Paroxetine hydrochloride
- Generic name
- Paroxetine hydrochloride
- Labeler
- Oxford Pharmaceuticals, LLC
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA076968
- Marketed since
- November 14, 2022
- Listing expires
- December 31, 2026
- Pharmacologic class
- Serotonin Reuptake Inhibitor
Active ingredients
- Paroxetine Hydrochloride 20 mg/1
Uses, dosage, side effects and warnings for Paroxetine Hydrochloride →
Package NDC codes (5)
| Package NDC | Description | Since |
|---|---|---|
| 69584-672-03 | 30 TABLET, FILM COATED in 1 BOTTLE (69584-672-03) | Nov 14, 2022 |
| 69584-672-09 | 90 TABLET, FILM COATED in 1 BOTTLE (69584-672-09) | Nov 14, 2022 |
| 69584-672-10 | 100 TABLET, FILM COATED in 1 BOTTLE (69584-672-10) | Nov 14, 2022 |
| 69584-672-50 | 500 TABLET, FILM COATED in 1 BOTTLE (69584-672-50) | Nov 14, 2022 |
| 69584-672-90 | 1000 TABLET, FILM COATED in 1 BOTTLE (69584-672-90) | Nov 14, 2022 |
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