NDC 27808-093 – Dexmethylphenidate Hydrochloride
Dexmethylphenidate Hydrochloride 10 mg/1 · Tablet · Oral
Product NDC27808-093
Product details
- Brand name
- Dexmethylphenidate Hydrochloride
- Generic name
- Dexmethylphenidate hydrochloride
- Labeler
- Cranbury Pharmaceuticals, LLC
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA207901
- Marketed since
- November 30, 2001
- Listing expires
- December 31, 2026
- Pharmacologic class
- Central Nervous System Stimulant
Active ingredients
- Dexmethylphenidate Hydrochloride 10 mg/1
Uses, dosage, side effects and warnings for Dexmethylphenidate Hydrochloride →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 27808-093-01 | 100 TABLET in 1 BOTTLE (27808-093-01) | Nov 30, 2001 |
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