NDC 57664-229 – Methylphenidate Hydrochloride
Methylphenidate Hydrochloride 10 mg/1 · Tablet · Oral
Product NDC57664-229
Product details
- Brand name
- Methylphenidate Hydrochloride
- Generic name
- Methylphenidate Hydrochloride
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA090710
- Marketed since
- August 16, 2013
- 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 (5)
| Package NDC | Description | Since |
|---|---|---|
| 57664-229-08 | 100 TABLET in 1 BOTTLE (57664-229-08) | Aug 16, 2013 |
| 57664-229-13 | 500 TABLET in 1 BOTTLE (57664-229-13) | Aug 16, 2013 |
| 57664-229-18 | 1000 TABLET in 1 BOTTLE (57664-229-18) | Aug 16, 2013 |
| 57664-229-83 | 30 TABLET in 1 BOTTLE (57664-229-83) | Aug 16, 2013 |
| 57664-229-88 | 100 TABLET in 1 BOTTLE (57664-229-88) | Aug 16, 2013 |
Recalls mentioning this NDC
- D-0940-2023 Aug 2, 2023 · Class II
Presence of Foreign Substance: Metal embedded in a tablet.
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