Product NDC: | 53014-579 |
Proprietary Name: | Metadate CD |
Non Proprietary Name: | methylphenidate hydrochloride |
Active Ingredient(s): | 10 mg/1 & nbsp; methylphenidate hydrochloride |
Administration Route(s): | ORAL |
Dosage Form(s): | CAPSULE, EXTENDED RELEASE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 53014-579 |
Labeler Name: | UCB Manufacturing, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA021259 |
Marketing Category: | NDA |
Start Marketing Date: | 20030812 |
Package NDC: | 53014-579-07 |
Package Description: | 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (53014-579-07) |
NDC Code | 53014-579-07 |
Proprietary Name | Metadate CD |
Package Description | 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (53014-579-07) |
Product NDC | 53014-579 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | methylphenidate hydrochloride |
Dosage Form Name | CAPSULE, EXTENDED RELEASE |
Route Name | ORAL |
Start Marketing Date | 20030812 |
Marketing Category Name | NDA |
Labeler Name | UCB Manufacturing, Inc. |
Substance Name | METHYLPHENIDATE HYDROCHLORIDE |
Strength Number | 10 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Central Nervous System Stimulant [EPC],Central Nervous System Stimulation [PE] |