NDC 13811-710 – Methylphenidate Hydrochloride
Methylphenidate Hydrochloride 72 mg/1 · Tablet, Extended Release · Oral
Product NDC13811-710
Product details
- Brand name
- Methylphenidate Hydrochloride
- Generic name
- Methylphenidate hydrochloride
- Labeler
- Trigen Laboratories, LLC
- Dosage form
- Tablet, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA205327
- Marketed since
- December 29, 2017
- 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 |
|---|---|---|
| 13811-710-10 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (13811-710-10) | Dec 29, 2017 |
| 13811-710-30 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (13811-710-30) | Dec 29, 2017 |
Recalls mentioning this NDC
- D-0579-2024 Jul 10, 2024 · Class II
Failed dissolution specifications: this product is being recalled due to this batch not meeting dissolution specifications. - D-0581-2018 Mar 14, 2018 · Class III
Subpotent Drug:100-count product bottle labeled as Methylphenidate HCL ER Tablets 36 mg found to contain 1 27 mg Methylphenidate HCL ER Tablet. - D-0110-2018 Dec 27, 2017 · Class III
Subpotent Drug - D-0111-2018 Dec 27, 2017 · Class III
Subpotent Drug
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