NDC 68382-098 – Paroxetine
Paroxetine Hydrochloride Hemihydrate 20 mg/1 · Tablet, Film Coated · Oral
Product NDC68382-098
Product details
- Brand name
- Paroxetine
- Generic name
- Paroxetine
- Labeler
- Zydus Pharmaceuticals USA Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA077584
- Marketed since
- April 13, 2007
- Listing expires
- December 31, 2026
- Pharmacologic class
- Serotonin Reuptake Inhibitor
Active ingredients
Package NDC codes (5)
| Package NDC | Description | Since |
|---|---|---|
| 68382-098-01 | 100 TABLET, FILM COATED in 1 BOTTLE (68382-098-01) | Apr 13, 2007 |
| 68382-098-05 | 500 TABLET, FILM COATED in 1 BOTTLE (68382-098-05) | Apr 13, 2007 |
| 68382-098-06 | 30 TABLET, FILM COATED in 1 BOTTLE (68382-098-06) | Apr 13, 2007 |
| 68382-098-10 | 1000 TABLET, FILM COATED in 1 BOTTLE (68382-098-10) | Apr 13, 2007 |
| 68382-098-16 | 90 TABLET, FILM COATED in 1 BOTTLE (68382-098-16) | Apr 13, 2007 |
Recalls mentioning this NDC
- D-0101-2018 Dec 6, 2017 · Class II
Presence of Foreign Tablets/Capsules: Risperidone Tablets were found in bottle of Paroxetine Tablets - D-1137-2017 Sep 20, 2017 · Class II
Presence of Foreign tablets/capsules: risperidone Tablets were found in bottle of paroxetine Tablets
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