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Potassium Chloride
Potassium Chloride - 52125-352-02 - (Potassium Chloride)
Drug Information of Potassium Chloride
| Product NDC: | 52125-352 |
| Proprietary Name: | Potassium Chloride |
| Non Proprietary Name: | Potassium Chloride |
| Active Ingredient(s): | 750 mg/1 & nbsp; Potassium Chloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Potassium Chloride
| Product NDC: | 52125-352 |
| Labeler Name: | REMEDYREPACK INC. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA018279 |
| Marketing Category: | NDA AUTHORIZED GENERIC |
| Start Marketing Date: | 20130528 |
Package Information of Potassium Chloride
| Package NDC: | 52125-352-02 |
| Package Description: | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (52125-352-02) |
NDC Information of Potassium Chloride
| NDC Code | 52125-352-02 |
| Proprietary Name | Potassium Chloride |
| Package Description | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (52125-352-02) |
| Product NDC | 52125-352 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Potassium Chloride |
| Dosage Form Name | TABLET, FILM COATED, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20130528 |
| Marketing Category Name | NDA AUTHORIZED GENERIC |
| Labeler Name | REMEDYREPACK INC. |
| Substance Name | POTASSIUM CHLORIDE |
| Strength Number | 750 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Potassium Compounds [Chemical/Ingredient],Potassium Salt [EPC] |
