| NDC Code | 60687-466-01 |
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| Package Description | 100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-466-01) > 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (60687-466-11) |
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| Product NDC | 60687-466 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Potassium Chloride |
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| Non-Proprietary Name | Potassium Chloride |
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| Dosage Form | TABLET, FILM COATED, EXTENDED RELEASE |
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| Usage | ORAL |
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| Start Marketing Date | 20190726 |
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| End Marketing Date | 20230731 |
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| Marketing Category Name | NDA AUTHORIZED GENERIC |
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| Application Number | NDA018279 |
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| Manufacturer | American Health Packaging |
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| Substance Name | POTASSIUM CHLORIDE |
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| Strength | 750 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Osmotic Activity [MoA], Osmotic Laxative [EPC], Potassium Compounds [CS], Potassium Salt [EPC] |
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