NDC 57664-710 – Methylphenidate Hydrochloride
Methylphenidate Hydrochloride 72 mg/1 · Tablet, Extended Release · Oral
Product NDC57664-710
Product details
- Brand name
- Methylphenidate Hydrochloride
- Generic name
- Methylphenidate Hydrochloride
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Dosage form
- Tablet, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA217229
- Marketed since
- December 20, 2024
- Listing expires
- December 31, 2027
- Pharmacologic class
- Central Nervous System Stimulant
Active ingredients
- Methylphenidate Hydrochloride 72 mg/1
Uses, dosage, side effects and warnings for Methylphenidate Hydrochloride →
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 57664-710-83 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (57664-710-83) | Dec 20, 2024 |
| 57664-710-88 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (57664-710-88) | Dec 20, 2024 |
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