NDC 75907-050 – Methylphenidate Hydrochloride (LA)
Methylphenidate Hydrochloride 20 mg/1 · Capsule, Extended Release · Oral
Product NDC75907-050
Product details
- Brand name
- Methylphenidate Hydrochloride (LA)
- Generic name
- Methylphenidate Hydrochloride
- Labeler
- Dr. Reddy's Laboratories Inc
- Dosage form
- Capsule, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA078458
- Marketed since
- December 20, 2024
- 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 (LA) →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 75907-050-01 | 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (75907-050-01) | Dec 20, 2024 |
Other Methylphenidate Hydrochloride (LA) products
- 75907-049 Methylphenidate Hydrochloride 10 mg/1 · Capsule, Extended Release · Dr. Reddy's Laboratories Inc
- 75907-051 Methylphenidate Hydrochloride 30 mg/1 · Capsule, Extended Release · Dr. Reddy's Laboratories Inc
- 75907-052 Methylphenidate Hydrochloride 40 mg/1 · Capsule, Extended Release · Dr. Reddy's Laboratories Inc
- 75907-053 Methylphenidate Hydrochloride 60 mg/1 · Capsule, Extended Release · Dr. Reddy's Laboratories Inc