NDC 43386-861 – Dexmethylphenidate Hydrochloride
Dexmethylphenidate Hydrochloride 10 mg/1 · Tablet · Oral
Product NDC43386-861
Product details
- Brand name
- Dexmethylphenidate Hydrochloride
- Generic name
- Dexmethylphenidate Hydrochloride
- Labeler
- Lupin Pharmaceuticals,Inc.
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA204534
- Marketed since
- December 4, 2015
- 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 |
|---|---|---|
| 43386-861-01 | 100 TABLET in 1 BOTTLE (43386-861-01) | Dec 4, 2015 |
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