NDC 0115-9921 – Dexmethylphenidate hydrochloride
Dexmethylphenidate Hydrochloride 20 mg/1 · Capsule, Extended Release · Oral
Product NDC0115-9921
Product details
- Brand name
- Dexmethylphenidate hydrochloride
- Generic name
- Dexmethylphenidate hydrochloride
- Labeler
- Amneal Pharmaceuticals of New York LLC
- Dosage form
- Capsule, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA079108
- Marketed since
- December 21, 2015
- Listing expires
- December 31, 2027
- 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 |
|---|---|---|
| 0115-9921-01 | 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0115-9921-01) | Dec 21, 2015 |
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