NDC 0115-1802 – Methylphenidate Hydrochloride
Methylphenidate Hydrochloride 20 mg/1 · Tablet · Oral
Product NDC0115-1802
Product details
- Brand name
- Methylphenidate Hydrochloride
- Generic name
- Methylphenidate Hydrochloride
- Labeler
- Amneal Pharmaceuticals of New York LLC
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA091159
- Marketed since
- April 7, 2014
- Listing expires
- December 31, 2026
- Pharmacologic class
- Central Nervous System Stimulant
Active ingredients
- Methylphenidate Hydrochloride 20 mg/1
Uses, dosage, side effects and warnings for Methylphenidate Hydrochloride →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 0115-1802-01 | 100 TABLET in 1 BOTTLE, PLASTIC (0115-1802-01) | Apr 7, 2014 |
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