Details for New Drug Application (NDA): 206049
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The generic ingredient in METHYLPHENIDATE HYDROCHLORIDE is methylphenidate hydrochloride. There are thirty-two drug master file entries for this compound. Forty-five suppliers are listed for this compound. Additional details are available on the methylphenidate hydrochloride profile page.
Summary for 206049
| Tradename: | METHYLPHENIDATE HYDROCHLORIDE |
| Applicant: | Actavis Labs Fl Inc |
| Ingredient: | methylphenidate hydrochloride |
| Patents: | 0 |
Profile for product number 001
| Active Rx/OTC/Discontinued: | RX | Dosage: | FOR SUSPENSION, EXTENDED RELEASE;ORAL | Strength | 5MG/ML | ||||
| Approval Date: | May 17, 2018 | TE: | AB | RLD: | No | ||||
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