| NDC Code | 60687-685-32 |
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| Package Description | 20 BLISTER PACK in 1 CARTON (60687-685-32) / 1 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (60687-685-33) |
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| Product NDC | 60687-685 |
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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 | 20230119 |
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| End Marketing Date | 20241031 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA078540 |
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| Manufacturer | American Health Packaging |
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| Substance Name | PROPAFENONE HYDROCHLORIDE |
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| Strength | 325 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Antiarrhythmic [EPC] |
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