NDC 51672-1348 – Escitalopram
Escitalopram Oxalate 5 mg/5mL · Solution · Oral
Product NDC51672-1348
Product details
- Brand name
- Escitalopram
- Generic name
- Escitalopram Oxalate
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Dosage form
- Solution
- Route
- Oral
- Marketing category
- ANDA · ANDA079121
- Marketed since
- May 3, 2012
- Listing expires
- December 31, 2026
- Pharmacologic class
- Serotonin Reuptake Inhibitor
Active ingredients
- Escitalopram Oxalate 5 mg/5mL
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 51672-1348-1 | 1 BOTTLE in 1 CARTON (51672-1348-1) / 240 mL in 1 BOTTLE | May 3, 2012 |
| 51672-1348-8 | 1 BOTTLE in 1 CARTON (51672-1348-8) / 120 mL in 1 BOTTLE | May 3, 2012 |
| 51672-1348-9 | 1 BOTTLE in 1 CARTON (51672-1348-9) / 480 mL in 1 BOTTLE | May 3, 2012 |
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