Product NDC: | 59630-761 |
Proprietary Name: | METHYLIN |
Non Proprietary Name: | methylphenidate hydrochloride |
Active Ingredient(s): | 5 mg/1 & nbsp; methylphenidate hydrochloride |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, CHEWABLE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 59630-761 |
Labeler Name: | SHIONOGI INC. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA021475 |
Marketing Category: | NDA |
Start Marketing Date: | 20101101 |
Package NDC: | 59630-761-10 |
Package Description: | 100 TABLET, CHEWABLE in 1 BOTTLE (59630-761-10) |
NDC Code | 59630-761-10 |
Proprietary Name | METHYLIN |
Package Description | 100 TABLET, CHEWABLE in 1 BOTTLE (59630-761-10) |
Product NDC | 59630-761 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | methylphenidate hydrochloride |
Dosage Form Name | TABLET, CHEWABLE |
Route Name | ORAL |
Start Marketing Date | 20101101 |
Marketing Category Name | NDA |
Labeler Name | SHIONOGI INC. |
Substance Name | METHYLPHENIDATE HYDROCHLORIDE |
Strength Number | 5 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Central Nervous System Stimulant [EPC],Central Nervous System Stimulation [PE] |