NDC 71335-2968 – Methylphenidate Hydrochloride
Methylphenidate Hydrochloride 10 mg/1 · Tablet · Oral
Product NDC71335-2968
Product details
- Brand name
- Methylphenidate Hydrochloride
- Generic name
- Methylphenidate Hydrochloride
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA208737
- Marketed since
- April 16, 2024
- Listing expires
- December 31, 2026
- Pharmacologic class
- Central Nervous System Stimulant
Active ingredients
- Methylphenidate Hydrochloride 10 mg/1
Uses, dosage, side effects and warnings for Methylphenidate Hydrochloride →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 71335-2968-1 | 100 TABLET in 1 BOTTLE (71335-2968-1) | Nov 11, 2025 |
Other Methylphenidate Hydrochloride products
- 16729-478 Methylphenidate Hydrochloride 5 mg/1 · Tablet · Accord Healthcare, Inc.
- 16729-480 Methylphenidate Hydrochloride 20 mg/1 · Tablet · Accord Healthcare, Inc.
- 16729-479 Methylphenidate Hydrochloride 10 mg/1 · Tablet · Accord Healthcare, Inc.
- 68084-805 Methylphenidate Hydrochloride 5 mg/1 · Tablet · American Health Packaging
- 68084-823 Methylphenidate Hydrochloride 10 mg/1 · Tablet · American Health Packaging
- 0115-1800 Methylphenidate Hydrochloride 5 mg/1 · Tablet · Amneal Pharmaceuticals of New York LLC
- 0115-1801 Methylphenidate Hydrochloride 10 mg/1 · Tablet · Amneal Pharmaceuticals of New York LLC
- 0115-1802 Methylphenidate Hydrochloride 20 mg/1 · Tablet · Amneal Pharmaceuticals of New York LLC
- 67877-616 Methylphenidate Hydrochloride 5 mg/1 · Tablet · Ascend Laboratories, LLC
- 67877-617 Methylphenidate Hydrochloride 10 mg/1 · Tablet · Ascend Laboratories, LLC
- 67877-618 Methylphenidate Hydrochloride 20 mg/1 · Tablet · Ascend Laboratories, LLC
- 13107-382 Methylphenidate Hydrochloride 20 mg/1 · Tablet · Aurolife Pharma, LLC