NDC 70010-043 – Methylphenidate Hydrochloride
Methylphenidate Hydrochloride 20 mg/1 · Tablet, Extended Release · Oral
Product NDC70010-043
Product details
- Brand name
- Methylphenidate Hydrochloride
- Generic name
- Methylphenidate Hydrochloride
- Labeler
- Granules Pharmaceuticals Inc.
- Dosage form
- Tablet, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA210992
- Marketed since
- December 17, 2018
- Listing expires
- December 31, 2027
- 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 (2)
| Package NDC | Description | Since |
|---|---|---|
| 70010-043-01 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70010-043-01) | Dec 17, 2018 |
| 70010-043-03 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70010-043-03) | Oct 31, 2022 |
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