| NDC Code | 57664-229-88 |
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| Package Description | 100 TABLET in 1 BOTTLE (57664-229-88) |
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| Product NDC | 57664-229 |
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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 | 20130816 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA090710 |
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| Manufacturer | Sun Pharmaceutical Industries, Inc. |
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| Substance Name | METHYLPHENIDATE HYDROCHLORIDE |
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| Strength | 10 |
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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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