Details for New Drug Application (NDA): 212697
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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-six suppliers are listed for this compound. Additional details are available on the methylphenidate hydrochloride profile page.
Summary for 212697
Tradename: | METHYLPHENIDATE HYDROCHLORIDE |
Applicant: | Prinston Inc |
Ingredient: | methylphenidate hydrochloride |
Patents: | 0 |
Pharmacology for NDA: 212697
Physiological Effect | Central Nervous System Stimulation |
Suppliers and Packaging for NDA: 212697
Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
---|---|---|---|---|---|---|---|---|
METHYLPHENIDATE HYDROCHLORIDE | methylphenidate hydrochloride | TABLET;ORAL | 212697 | ANDA | Solco Healthcare US,LLC | 43547-486 | 43547-486-10 | 100 TABLET in 1 BOTTLE (43547-486-10) |
METHYLPHENIDATE HYDROCHLORIDE | methylphenidate hydrochloride | TABLET;ORAL | 212697 | ANDA | Solco Healthcare US,LLC | 43547-487 | 43547-487-10 | 100 TABLET in 1 BOTTLE (43547-487-10) |
Profile for product number 001
Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 5MG | ||||
Approval Date: | Jul 23, 2020 | TE: | AB | RLD: | No |
Profile for product number 002
Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 10MG | ||||
Approval Date: | Jul 23, 2020 | TE: | AB | RLD: | No |
Profile for product number 003
Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 20MG | ||||
Approval Date: | Jul 23, 2020 | TE: | AB | RLD: | No |
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