NDC 68788-7461 – Escitalopram
Escitalopram Oxalate 20 mg/1 · Tablet, Film Coated · Oral
Product NDC68788-7461
Product details
- Brand name
- Escitalopram
- Generic name
- Escitalopram
- Labeler
- Preferred Pharmaceuticals, Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA078032
- Marketed since
- March 15, 2012
- Listing expires
- December 31, 2027
- Pharmacologic class
- Serotonin Reuptake Inhibitor
Active ingredients
- Escitalopram Oxalate 20 mg/1
Package NDC codes (5)
| Package NDC | Description | Since |
|---|---|---|
| 68788-7461-1 | 100 TABLET, FILM COATED in 1 BOTTLE (68788-7461-1) | Dec 27, 2019 |
| 68788-7461-3 | 30 TABLET, FILM COATED in 1 BOTTLE (68788-7461-3) | Dec 27, 2019 |
| 68788-7461-6 | 60 TABLET, FILM COATED in 1 BOTTLE (68788-7461-6) | Dec 27, 2019 |
| 68788-7461-8 | 28 TABLET, FILM COATED in 1 BOTTLE (68788-7461-8) | Dec 27, 2019 |
| 68788-7461-9 | 90 TABLET, FILM COATED in 1 BOTTLE (68788-7461-9) | Dec 27, 2019 |
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