NDC 16714-612 – Sertraline Hydrochloride
Sertraline Hydrochloride 50 mg/1 · Tablet, Film Coated · Oral
Product NDC16714-612
Product details
- Brand name
- Sertraline Hydrochloride
- Generic name
- Sertraline Hydrochloride
- Labeler
- NorthStar Rx LLC
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA077206
- Marketed since
- February 6, 2007
- Listing expires
- December 31, 2026
- Pharmacologic class
- Serotonin Reuptake Inhibitor
Active ingredients
- Sertraline Hydrochloride 50 mg/1
Uses, dosage, side effects and warnings for Sertraline hydrochloride →
Package NDC codes (6)
| Package NDC | Description | Since |
|---|---|---|
| 16714-612-01 | 30 TABLET, FILM COATED in 1 BOTTLE (16714-612-01) | Feb 6, 2007 |
| 16714-612-02 | 60 TABLET, FILM COATED in 1 BOTTLE (16714-612-02) | Feb 6, 2007 |
| 16714-612-03 | 90 TABLET, FILM COATED in 1 BOTTLE (16714-612-03) | Feb 6, 2007 |
| 16714-612-04 | 100 TABLET, FILM COATED in 1 BOTTLE (16714-612-04) | Feb 6, 2007 |
| 16714-612-05 | 500 TABLET, FILM COATED in 1 BOTTLE (16714-612-05) | Feb 6, 2007 |
| 16714-612-06 | 1000 TABLET, FILM COATED in 1 BOTTLE (16714-612-06) | Feb 6, 2007 |
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