| NDC Code | 16571-736-50 |
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| Package Description | 500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (16571-736-50) |
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| Product NDC | 16571-736 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Propafenone Hydrochloride |
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| Non-Proprietary Name | Propafenone Hydrochloride |
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| Dosage Form | CAPSULE, EXTENDED RELEASE |
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| Usage | ORAL |
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| Start Marketing Date | 20201216 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA205956 |
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| Manufacturer | Rising Pharma Holdings, Inc. |
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| Substance Name | PROPAFENONE HYDROCHLORIDE |
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| Strength | 225 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Antiarrhythmic [EPC] |
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