Details for New Drug Application (NDA): 207485
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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-seven suppliers are listed for this compound. Additional details are available on the methylphenidate hydrochloride profile page.
Summary for 207485
Tradename: | METHYLPHENIDATE HYDROCHLORIDE |
Applicant: | Abhai Llc |
Ingredient: | methylphenidate hydrochloride |
Patents: | 0 |
Pharmacology for NDA: 207485
Physiological Effect | Central Nervous System Stimulation |
Suppliers and Packaging for NDA: 207485
Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
---|---|---|---|---|---|---|---|---|
METHYLPHENIDATE HYDROCHLORIDE | methylphenidate hydrochloride | SOLUTION;ORAL | 207485 | ANDA | KVK-Tech, Inc. | 10702-163 | 10702-163-50 | 500 mL in 1 BOTTLE (10702-163-50) |
METHYLPHENIDATE HYDROCHLORIDE | methylphenidate hydrochloride | SOLUTION;ORAL | 207485 | ANDA | KVK-Tech, Inc. | 10702-164 | 10702-164-50 | 500 mL in 1 BOTTLE (10702-164-50) |
Profile for product number 001
Active Rx/OTC/Discontinued: | RX | Dosage: | SOLUTION;ORAL | Strength | 5MG/5ML | ||||
Approval Date: | Nov 18, 2016 | TE: | AA | RLD: | No |
Profile for product number 002
Active Rx/OTC/Discontinued: | RX | Dosage: | SOLUTION;ORAL | Strength | 10MG/5ML | ||||
Approval Date: | Nov 18, 2016 | TE: | AA | RLD: | No |
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