NDC 13107-154 – Paroxetine
Paroxetine Hydrochloride Hemihydrate 10 mg/1 · Tablet, Film Coated · Oral
Product NDC13107-154
Product details
- Brand name
- Paroxetine
- Generic name
- Paroxetine
- Labeler
- Aurolife Pharma LLC
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA078406
- Marketed since
- December 3, 2009
- Listing expires
- December 31, 2026
- Pharmacologic class
- Serotonin Reuptake Inhibitor
Active ingredients
Package NDC codes (5)
| Package NDC | Description | Since |
|---|---|---|
| 13107-154-01 | 100 TABLET, FILM COATED in 1 BOTTLE (13107-154-01) | Dec 3, 2009 |
| 13107-154-05 | 500 TABLET, FILM COATED in 1 BOTTLE (13107-154-05) | Dec 3, 2009 |
| 13107-154-30 | 30 TABLET, FILM COATED in 1 BOTTLE (13107-154-30) | Dec 3, 2009 |
| 13107-154-90 | 90 TABLET, FILM COATED in 1 BOTTLE (13107-154-90) | Dec 3, 2009 |
| 13107-154-99 | 1000 TABLET, FILM COATED in 1 BOTTLE (13107-154-99) | Dec 3, 2009 |
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