NDC 68180-353 – Sertraline Hydrochloride
Sertraline Hydrochloride 100 mg/1 · Tablet, Film Coated · Oral
Product NDC68180-353
Product details
- Brand name
- Sertraline Hydrochloride
- Generic name
- Sertraline Hydrochloride
- Labeler
- Lupin Pharmaceuticals, Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA077670
- Marketed since
- February 6, 2007
- Listing expires
- December 31, 2027
- Pharmacologic class
- Serotonin Reuptake Inhibitor
Active ingredients
- Sertraline Hydrochloride 100 mg/1
Uses, dosage, side effects and warnings for Sertraline hydrochloride →
Package NDC codes (4)
| Package NDC | Description | Since |
|---|---|---|
| 68180-353-02 | 500 TABLET, FILM COATED in 1 BOTTLE (68180-353-02) | Feb 6, 2007 |
| 68180-353-05 | 5000 TABLET, FILM COATED in 1 BOTTLE (68180-353-05) | Feb 6, 2007 |
| 68180-353-06 | 30 TABLET, FILM COATED in 1 BOTTLE (68180-353-06) | Feb 6, 2007 |
| 68180-353-09 | 90 TABLET, FILM COATED in 1 BOTTLE (68180-353-09) | Feb 6, 2007 |
Recalls mentioning this NDC
- D-0227-2026 Dec 17, 2025 · Class II
Defective container - seal not adhering to bottles
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