| NDC Code | 48102-111-30 |
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| Package Description | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (48102-111-30) |
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| Product NDC | 48102-111 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Amoxicillin Extended-release |
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| Non-Proprietary Name | Amoxicillin |
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| Dosage Form | TABLET, FILM COATED, EXTENDED RELEASE |
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| Usage | ORAL |
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| Start Marketing Date | 20140728 |
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| Marketing Category Name | NDA AUTHORIZED GENERIC |
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| Application Number | NDA050813 |
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| Manufacturer | Fera Pharmaceuticals, LLC |
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| Substance Name | AMOXICILLIN |
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| Strength | 775 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Penicillin-class Antibacterial [EPC],Penicillins [Chemical/Ingredient] |
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