| NDC Code | 63304-076-05 |
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| Package Description | 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (63304-076-05) |
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| Product NDC | 63304-076 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Potassium Chloride Extended-release |
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| Non-Proprietary Name | Potassium Chloride |
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| Dosage Form | TABLET, EXTENDED RELEASE |
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| Usage | ORAL |
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| Start Marketing Date | 20191120 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA076368 |
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| Manufacturer | Sun Pharmaceutical Industries, Inc. |
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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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