| NDC Code | 68084-829-25 |
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| Package Description | 30 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-829-25) > 1 TABLET in 1 BLISTER PACK (68084-829-95) |
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| Product NDC | 68084-829 |
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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 | TABLET |
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| Usage | ORAL |
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| Start Marketing Date | 20140821 |
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| End Marketing Date | 20200930 |
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| Marketing Category Name | NDA AUTHORIZED GENERIC |
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| Application Number | NDA021121 |
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| Manufacturer | American Health Packaging |
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| Substance Name | METHYLPHENIDATE HYDROCHLORIDE |
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| Strength | 36 |
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| Strength Unit | mg/1 |
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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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