NDC 68788-8569 – Escitalopram
Escitalopram Oxalate 10 mg/1 · Tablet, Film Coated · Oral
Product NDC68788-8569
Product details
- Brand name
- Escitalopram
- Generic name
- Escitalopram
- Labeler
- Preferred Pharmaceuticals Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA078777
- Marketed since
- January 23, 2024
- Listing expires
- December 31, 2027
- Pharmacologic class
- Serotonin Reuptake Inhibitor
Active ingredients
- Escitalopram Oxalate 10 mg/1
Package NDC codes (4)
| Package NDC | Description | Since |
|---|---|---|
| 68788-8569-1 | 100 TABLET, FILM COATED in 1 BOTTLE (68788-8569-1) | Apr 8, 2025 |
| 68788-8569-3 | 30 TABLET, FILM COATED in 1 BOTTLE (68788-8569-3) | Jan 23, 2024 |
| 68788-8569-6 | 60 TABLET, FILM COATED in 1 BOTTLE (68788-8569-6) | Apr 8, 2025 |
| 68788-8569-9 | 90 TABLET, FILM COATED in 1 BOTTLE (68788-8569-9) | Apr 8, 2025 |
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