Home
>
National Drug Code (NDC)
>
Methylphenidate Hydrochloride
Methylphenidate Hydrochloride - 51991-712-50 - (Methylphenidate Hydrochloride)
Drug Information of Methylphenidate Hydrochloride
| Product NDC: | 51991-712 |
| Proprietary Name: | Methylphenidate Hydrochloride |
| Non Proprietary Name: | Methylphenidate Hydrochloride |
| Active Ingredient(s): | 5 mg/5mL & nbsp; Methylphenidate Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Methylphenidate Hydrochloride
| Product NDC: | 51991-712 |
| Labeler Name: | Breckenridge Pharmaceutical, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA091601 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20100701 |
Package Information of Methylphenidate Hydrochloride
| Package NDC: | 51991-712-50 |
| Package Description: | 500 mL in 1 BOTTLE (51991-712-50) |
NDC Information of Methylphenidate Hydrochloride
| NDC Code | 51991-712-50 |
| Proprietary Name | Methylphenidate Hydrochloride |
| Package Description | 500 mL in 1 BOTTLE (51991-712-50) |
| Product NDC | 51991-712 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Methylphenidate Hydrochloride |
| Dosage Form Name | SOLUTION |
| Route Name | ORAL |
| Start Marketing Date | 20100701 |
| Marketing Category Name | ANDA |
| Labeler Name | Breckenridge Pharmaceutical, Inc. |
| Substance Name | METHYLPHENIDATE HYDROCHLORIDE |
| Strength Number | 5 |
| Strength Unit | mg/5mL |
| Pharmaceutical Classes | Central Nervous System Stimulant [EPC],Central Nervous System Stimulation [PE] |
