| NDC Code | 45963-807-11 |
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| Package Description | 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (45963-807-11) |
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| Product NDC | 45963-807 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Dexmethylphenidate Hydrochloride |
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| Non-Proprietary Name | Dexmethylphenidate Hydrochloride |
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| Dosage Form | CAPSULE, EXTENDED RELEASE |
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| Usage | ORAL |
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| Start Marketing Date | 20160215 |
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| End Marketing Date | 20170928 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA079108 |
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| Manufacturer | Actavis Pharma, Inc. |
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| Substance Name | DEXMETHYLPHENIDATE HYDROCHLORIDE |
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| Strength | 20 |
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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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