Details for New Drug Application (NDA): 210139
✉ Email this page to a colleague
The generic ingredient in METHYLPHENIDATE HYDROCHLORIDE is methylphenidate hydrochloride. There are thirty-two drug master file entries for this compound. Forty-six suppliers are listed for this compound. Additional details are available on the methylphenidate hydrochloride profile page.
Summary for 210139
Tradename: | METHYLPHENIDATE HYDROCHLORIDE |
Applicant: | Wes Pharma Inc |
Ingredient: | methylphenidate hydrochloride |
Patents: | 0 |
Pharmacology for NDA: 210139
Physiological Effect | Central Nervous System Stimulation |
Suppliers and Packaging for NDA: 210139
Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
---|---|---|---|---|---|---|---|---|
METHYLPHENIDATE HYDROCHLORIDE | methylphenidate hydrochloride | SOLUTION;ORAL | 210139 | ANDA | Bryant Ranch Prepack | 63629-1175 | 63629-1175-1 | 500 mL in 1 BOTTLE (63629-1175-1) |
METHYLPHENIDATE HYDROCHLORIDE | methylphenidate hydrochloride | SOLUTION;ORAL | 210139 | ANDA | Bryant Ranch Prepack | 63629-1176 | 63629-1176-1 | 500 mL in 1 BOTTLE (63629-1176-1) |
Profile for product number 001
Active Rx/OTC/Discontinued: | RX | Dosage: | SOLUTION;ORAL | Strength | 5MG/5ML | ||||
Approval Date: | Oct 3, 2018 | TE: | AA | RLD: | No |
Profile for product number 002
Active Rx/OTC/Discontinued: | RX | Dosage: | SOLUTION;ORAL | Strength | 10MG/5ML | ||||
Approval Date: | Oct 3, 2018 | TE: | AA | RLD: | No |
Complete Access Available with Subscription