| NDC Code | 57664-369-35 |
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| Package Description | 500 mL in 1 BOTTLE (57664-369-35) |
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| Product NDC | 57664-369 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Methylphenidate Hydrochloride |
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| Non-Proprietary Name | Methylphenidate Hydrochloride |
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| Dosage Form | SOLUTION |
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| Usage | ORAL |
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| Start Marketing Date | 20120301 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA201466 |
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| Manufacturer | Caraco Pharmaceutical Laboratories, Ltd. |
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| Substance Name | METHYLPHENIDATE HYDROCHLORIDE |
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| Strength | 5 |
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| Strength Unit | mg/5mL |
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| Pharmacy Classes | Central Nervous System Stimulant [EPC],Central Nervous System Stimulation [PE] |
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| DEA Schedule | CII |
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