NDC 53746-021 – Escitalopram Oxalate
Escitalopram Oxalate 20 mg/1 · Tablet, Film Coated · Oral
Product NDC53746-021
Product details
- Brand name
- Escitalopram Oxalate
- Generic name
- Escitalopram Oxalate
- Labeler
- Amneal Pharmaceuticals of New York LLC
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA205619
- Marketed since
- May 17, 2017
- Listing expires
- December 31, 2026
- Pharmacologic class
- Serotonin Reuptake Inhibitor
Active ingredients
- Escitalopram Oxalate 20 mg/1
Uses, dosage, side effects and warnings for Escitalopram oxalate →
Package NDC codes (4)
| Package NDC | Description | Since |
|---|---|---|
| 53746-021-05 | 500 TABLET, FILM COATED in 1 BOTTLE (53746-021-05) | May 17, 2017 |
| 53746-021-10 | 1000 TABLET, FILM COATED in 1 BOTTLE (53746-021-10) | May 17, 2017 |
| 53746-021-30 | 30 TABLET, FILM COATED in 1 BOTTLE (53746-021-30) | May 17, 2017 |
| 53746-021-90 | 90 TABLET, FILM COATED in 1 BOTTLE (53746-021-90) | May 17, 2017 |
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