| NDC Code | 0121-1792-20 |
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| Package Description | 2 TRAY in 1 CASE (0121-1792-20) > 10 CUP, UNIT-DOSE in 1 TRAY > 10 mL in 1 CUP, UNIT-DOSE (0121-1792-10) |
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| Product NDC | 0121-1792 |
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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 | 20200618 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA201466 |
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| Manufacturer | Pharmaceutical Associates, Inc. |
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| Substance Name | METHYLPHENIDATE HYDROCHLORIDE |
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| Strength | 10 |
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| Strength Unit | mg/10mL |
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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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