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Methylphenidate Hydrochloride
Methylphenidate Hydrochloride - 0781-5754-01 - (methylphenidate hydrochloride)
Drug Information of Methylphenidate Hydrochloride
| Product NDC: | 0781-5754 |
| Proprietary Name: | Methylphenidate Hydrochloride |
| Non Proprietary Name: | methylphenidate hydrochloride |
| Active Ingredient(s): | 20 mg/1 & nbsp; methylphenidate hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Methylphenidate Hydrochloride
| Product NDC: | 0781-5754 |
| Labeler Name: | Sandoz Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA018029 |
| Marketing Category: | NDA AUTHORIZED GENERIC |
| Start Marketing Date: | 19820331 |
Package Information of Methylphenidate Hydrochloride
| Package NDC: | 0781-5754-01 |
| Package Description: | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0781-5754-01) |
NDC Information of Methylphenidate Hydrochloride
| NDC Code | 0781-5754-01 |
| Proprietary Name | Methylphenidate Hydrochloride |
| Package Description | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0781-5754-01) |
| Product NDC | 0781-5754 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | methylphenidate hydrochloride |
| Dosage Form Name | TABLET, FILM COATED, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 19820331 |
| Marketing Category Name | NDA AUTHORIZED GENERIC |
| Labeler Name | Sandoz Inc |
| Substance Name | METHYLPHENIDATE HYDROCHLORIDE |
| Strength Number | 20 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Central Nervous System Stimulant [EPC],Central Nervous System Stimulation [PE] |
