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Quillivant
Quillivant - 24478-200-20 - (METHYLPHENIDATE HYDROCHLORIDE)
Drug Information of Quillivant
| Product NDC: | 24478-200 |
| Proprietary Name: | Quillivant |
| Non Proprietary Name: | METHYLPHENIDATE HYDROCHLORIDE |
| Active Ingredient(s): | 600 mg/120mL & nbsp; METHYLPHENIDATE HYDROCHLORIDE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | POWDER, FOR SUSPENSION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Quillivant
| Product NDC: | 24478-200 |
| Labeler Name: | NextWave Pharmaceuticals, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA202100 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20121001 |
Package Information of Quillivant
| Package NDC: | 24478-200-20 |
| Package Description: | 120 mL in 1 BOTTLE (24478-200-20) |
NDC Information of Quillivant
| NDC Code | 24478-200-20 |
| Proprietary Name | Quillivant |
| Package Description | 120 mL in 1 BOTTLE (24478-200-20) |
| Product NDC | 24478-200 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | METHYLPHENIDATE HYDROCHLORIDE |
| Dosage Form Name | POWDER, FOR SUSPENSION |
| Route Name | ORAL |
| Start Marketing Date | 20121001 |
| Marketing Category Name | NDA |
| Labeler Name | NextWave Pharmaceuticals, Inc. |
| Substance Name | METHYLPHENIDATE HYDROCHLORIDE |
| Strength Number | 600 |
| Strength Unit | mg/120mL |
| Pharmaceutical Classes | Central Nervous System Stimulant [EPC],Central Nervous System Stimulation [PE] |
