NDC 72865-135 – Methylphenidate Hydrochloride
Methylphenidate Hydrochloride 36 mg/1 · Tablet, Extended Release · Oral
Product NDC72865-135
Product details
- Brand name
- Methylphenidate Hydrochloride
- Generic name
- Methylphenidate Hydrochloride
- Labeler
- XLCare Pharmaceuticals, Inc.
- Dosage form
- Tablet, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA211009
- Marketed since
- February 24, 2020
- Listing expires
- December 31, 2026
- Pharmacologic class
- Central Nervous System Stimulant
Active ingredients
- Methylphenidate Hydrochloride 36 mg/1
Uses, dosage, side effects and warnings for Methylphenidate Hydrochloride →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 72865-135-01 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (72865-135-01) | Feb 24, 2020 |
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