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Concerta
Concerta - 54868-4789-0 - (Methylphenidate hydrochloride)
Drug Information of Concerta
| Product NDC: | 54868-4789 |
| Proprietary Name: | Concerta |
| Non Proprietary Name: | Methylphenidate hydrochloride |
| Active Ingredient(s): | 54 mg/1 & nbsp; Methylphenidate hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Concerta
| Product NDC: | 54868-4789 |
| Labeler Name: | Physicians Total Care, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021121 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20030508 |
Package Information of Concerta
| Package NDC: | 54868-4789-0 |
| Package Description: | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (54868-4789-0) |
NDC Information of Concerta
| NDC Code | 54868-4789-0 |
| Proprietary Name | Concerta |
| Package Description | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (54868-4789-0) |
| Product NDC | 54868-4789 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Methylphenidate hydrochloride |
| Dosage Form Name | TABLET, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20030508 |
| Marketing Category Name | NDA |
| Labeler Name | Physicians Total Care, Inc. |
| Substance Name | METHYLPHENIDATE HYDROCHLORIDE |
| Strength Number | 54 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Central Nervous System Stimulant [EPC],Central Nervous System Stimulation [PE] |
