NDC 65862-375 – Escitalopram
Escitalopram Oxalate 20 mg/1 · Tablet, Film Coated · Oral
Product NDC65862-375
Product details
- Brand name
- Escitalopram
- Generic name
- Escitalopram Oxalate
- Labeler
- Aurobindo Pharma Limited
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA090432
- Marketed since
- September 11, 2012
- Listing expires
- December 31, 2027
- Pharmacologic class
- Serotonin Reuptake Inhibitor
Active ingredients
- Escitalopram Oxalate 20 mg/1
Package NDC codes (6)
| Package NDC | Description | Since |
|---|---|---|
| 65862-375-01 | 100 TABLET, FILM COATED in 1 BOTTLE (65862-375-01) | Sep 11, 2012 |
| 65862-375-05 | 500 TABLET, FILM COATED in 1 BOTTLE (65862-375-05) | Sep 11, 2012 |
| 65862-375-10 | 10 BLISTER PACK in 1 CARTON (65862-375-10) / 10 TABLET, FILM COATED in 1 BLISTER PACK | Sep 11, 2012 |
| 65862-375-30 | 30 TABLET, FILM COATED in 1 BOTTLE (65862-375-30) | Sep 11, 2012 |
| 65862-375-39 | 3000 TABLET, FILM COATED in 1 BOTTLE (65862-375-39) | Sep 11, 2012 |
| 65862-375-90 | 90 TABLET, FILM COATED in 1 BOTTLE (65862-375-90) | Sep 11, 2012 |
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