| NDC Code | 61919-953-30 |
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| Package Description | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (61919-953-30) |
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| Product NDC | 61919-953 |
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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 | 20140101 |
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| Marketing Category Name | NDA AUTHORIZED GENERIC |
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| Application Number | NDA018279 |
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| Manufacturer | DIRECT RX |
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| Substance Name | POTASSIUM CHLORIDE |
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| Strength | 1500 |
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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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