Home
>
National Drug Code (NDC)
>
Methylphenidate
Methylphenidate - 54868-0733-2 - (Methylphenidate hydrochloride)
Drug Information of Methylphenidate
| Product NDC: | 54868-0733 |
| Proprietary Name: | Methylphenidate |
| Non Proprietary Name: | Methylphenidate hydrochloride |
| Active Ingredient(s): | 10 mg/1 & nbsp; Methylphenidate hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Methylphenidate
| Product NDC: | 54868-0733 |
| Labeler Name: | Physicians Total Care, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA040220 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20050324 |
Package Information of Methylphenidate
| Package NDC: | 54868-0733-2 |
| Package Description: | 20 TABLET in 1 BOTTLE (54868-0733-2) |
NDC Information of Methylphenidate
| NDC Code | 54868-0733-2 |
| Proprietary Name | Methylphenidate |
| Package Description | 20 TABLET in 1 BOTTLE (54868-0733-2) |
| Product NDC | 54868-0733 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Methylphenidate hydrochloride |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20050324 |
| Marketing Category Name | ANDA |
| Labeler Name | Physicians Total Care, Inc. |
| Substance Name | METHYLPHENIDATE HYDROCHLORIDE |
| Strength Number | 10 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Central Nervous System Stimulant [EPC],Central Nervous System Stimulation [PE] |
