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methylphenidate hydrochloride CD
methylphenidate hydrochloride CD - 62175-155-37 - (methylphenidate hydrochloride)
Drug Information of methylphenidate hydrochloride CD
| Product NDC: | 62175-155 |
| Proprietary Name: | methylphenidate hydrochloride CD |
| Non Proprietary Name: | methylphenidate hydrochloride |
| Active Ingredient(s): | 50 mg/1 & nbsp; methylphenidate hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of methylphenidate hydrochloride CD
| Product NDC: | 62175-155 |
| Labeler Name: | Kremers Urban Pharmaceuticals Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021259 |
| Marketing Category: | NDA AUTHORIZED GENERIC |
| Start Marketing Date: | 20060321 |
Package Information of methylphenidate hydrochloride CD
| Package NDC: | 62175-155-37 |
| Package Description: | 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (62175-155-37) |
NDC Information of methylphenidate hydrochloride CD
| NDC Code | 62175-155-37 |
| Proprietary Name | methylphenidate hydrochloride CD |
| Package Description | 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (62175-155-37) |
| Product NDC | 62175-155 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | methylphenidate hydrochloride |
| Dosage Form Name | CAPSULE, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20060321 |
| Marketing Category Name | NDA AUTHORIZED GENERIC |
| Labeler Name | Kremers Urban Pharmaceuticals Inc. |
| Substance Name | METHYLPHENIDATE HYDROCHLORIDE |
| Strength Number | 50 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Central Nervous System Stimulant [EPC],Central Nervous System Stimulation [PE] |
