NDC 57664-376 – Dexmethylphenidate hydrochloride
Dexmethylphenidate Hydrochloride 2.5 mg/1 · Tablet · Oral
Product NDC57664-376
Product details
- Brand name
- Dexmethylphenidate hydrochloride
- Generic name
- Dexmethylphenidate hydrochloride
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA201231
- Marketed since
- September 26, 2013
- Listing expires
- December 31, 2026
- Pharmacologic class
- Central Nervous System Stimulant
Active ingredients
- Dexmethylphenidate Hydrochloride 2.5 mg/1
Uses, dosage, side effects and warnings for Dexmethylphenidate Hydrochloride →
Package NDC codes (5)
| Package NDC | Description | Since |
|---|---|---|
| 57664-376-08 | 100 TABLET in 1 BOTTLE (57664-376-08) | Sep 26, 2013 |
| 57664-376-13 | 500 TABLET in 1 BOTTLE (57664-376-13) | Sep 26, 2013 |
| 57664-376-18 | 1000 TABLET in 1 BOTTLE (57664-376-18) | Sep 26, 2013 |
| 57664-376-83 | 30 TABLET in 1 BOTTLE (57664-376-83) | Sep 26, 2013 |
| 57664-376-88 | 100 TABLET in 1 BOTTLE (57664-376-88) | Sep 26, 2013 |
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