| NDC Code | 68084-933-32 |
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| Package Description | 20 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-933-32) > 1 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (68084-933-33) |
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| Product NDC | 68084-933 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Dexmethylphenidate Hydrochloride Extended-release |
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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 | 20150331 |
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| End Marketing Date | 20180630 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA078992 |
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| Manufacturer | American Health Packaging |
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| Substance Name | DEXMETHYLPHENIDATE HYDROCHLORIDE |
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| Strength | 30 |
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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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