| NDC Code | 51991-712-50 |
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| Package Description | 500 mL in 1 BOTTLE (51991-712-50) |
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| Product NDC | 51991-712 |
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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 | 20100701 |
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| End Marketing Date | 20190630 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA091601 |
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| Manufacturer | Breckenridge Pharmaceutical, Inc. |
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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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