NDC 71335-1219 – Methylphenidate Hydrochloride
Methylphenidate Hydrochloride 20 mg/1 · Tablet · Oral
Product NDC71335-1219
Product details
- Brand name
- Methylphenidate Hydrochloride
- Generic name
- Methylphenidate Hydrochloride
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA207416
- Marketed since
- October 1, 2015
- 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 →
Package NDC codes (5)
| Package NDC | Description | Since |
|---|---|---|
| 71335-1219-1 | 30 TABLET in 1 BOTTLE (71335-1219-1) | Oct 31, 2024 |
| 71335-1219-2 | 100 TABLET in 1 BOTTLE (71335-1219-2) | Oct 31, 2024 |
| 71335-1219-3 | 90 TABLET in 1 BOTTLE (71335-1219-3) | Apr 24, 2019 |
| 71335-1219-4 | 60 TABLET in 1 BOTTLE (71335-1219-4) | Apr 24, 2019 |
| 71335-1219-5 | 120 TABLET in 1 BOTTLE (71335-1219-5) | Oct 31, 2024 |
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