NDC 0781-2730 – Dexmethylphenidate Hydrochloride Extended-Release
Dexmethylphenidate Hydrochloride 20 mg/1 · Capsule, Extended Release · Oral
Product NDC0781-2730
Product details
- Brand name
- Dexmethylphenidate Hydrochloride Extended-Release
- Generic name
- dexmethylphenidate hydrochloride
- Labeler
- Sandoz Inc
- Dosage form
- Capsule, Extended Release
- Route
- Oral
- Marketing category
- NDA AUTHORIZED GENERIC · NDA021802
- Marketed since
- September 24, 2026
- Pharmacologic class
- Central Nervous System Stimulant
Active ingredients
- Dexmethylphenidate Hydrochloride 20 mg/1
Uses, dosage, side effects and warnings for Dexmethylphenidate Hydrochloride →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 0781-2730-31 | 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0781-2730-31) | Sep 24, 2026 |
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