NDC 68788-8371 – Escitalopram oxalate
Escitalopram Oxalate 10 mg/1 · Tablet, Film Coated · Oral
Product NDC68788-8371
Product details
- Brand name
- Escitalopram oxalate
- Generic name
- Escitalopram oxalate
- Labeler
- Preferred Pharmaceuticals Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA090939
- Marketed since
- February 1, 2023
- Listing expires
- December 31, 2027
- Pharmacologic class
- Serotonin Reuptake Inhibitor
Active ingredients
- Escitalopram Oxalate 10 mg/1
Uses, dosage, side effects and warnings for Escitalopram oxalate →
Package NDC codes (5)
| Package NDC | Description | Since |
|---|---|---|
| 68788-8371-1 | 100 TABLET, FILM COATED in 1 BOTTLE (68788-8371-1) | Feb 1, 2023 |
| 68788-8371-3 | 30 TABLET, FILM COATED in 1 BOTTLE (68788-8371-3) | Feb 1, 2023 |
| 68788-8371-6 | 60 TABLET, FILM COATED in 1 BOTTLE (68788-8371-6) | Feb 1, 2023 |
| 68788-8371-8 | 28 TABLET, FILM COATED in 1 BOTTLE (68788-8371-8) | Feb 1, 2023 |
| 68788-8371-9 | 90 TABLET, FILM COATED in 1 BOTTLE (68788-8371-9) | Feb 1, 2023 |
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