NDC 67877-656 – Dexmethylphenidate Hydrochloride
Dexmethylphenidate Hydrochloride 5 mg/1 · Tablet · Oral
Product NDC67877-656
Product details
- Brand name
- Dexmethylphenidate Hydrochloride
- Generic name
- Dexmethylphenidate Hydrochloride
- Labeler
- Ascend Laboratories, LLC
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA212631
- Marketed since
- July 21, 2019
- Listing expires
- December 31, 2026
- Pharmacologic class
- Central Nervous System Stimulant
Active ingredients
Uses, dosage, side effects and warnings for Dexmethylphenidate Hydrochloride →
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 67877-656-01 | 100 TABLET in 1 BOTTLE (67877-656-01) | Jul 21, 2019 |
| 67877-656-05 | 500 TABLET in 1 BOTTLE (67877-656-05) | Jul 21, 2019 |
| 67877-656-30 | 30 TABLET in 1 BOTTLE (67877-656-30) | Jul 21, 2019 |
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