| NDC Code | 49884-720-11 |
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| Package Description | 30 TABLET in 1 BOTTLE (49884-720-11) |
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| Product NDC | 49884-720 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Sapropterin Dihydrochloride |
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| Non-Proprietary Name | Sapropterin Dihydrochloride |
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| Dosage Form | TABLET |
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| Usage | ORAL |
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| Start Marketing Date | 20170202 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA207200 |
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| Manufacturer | Par Pharmaceutical, Inc. |
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| Substance Name | SAPROPTERIN DIHYDROCHLORIDE |
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| Strength | 100 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Phenylalanine Hydroxylase Activator [EPC],Phenylalanine Hydroxylase Activators [MoA],Breast Cancer Resistance Protein Inhibitors [MoA],P-Glycoprotein Inhibitors [MoA] |
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