Product NDC: | 52125-098 |
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, EXTENDED RELEASE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 52125-098 |
Labeler Name: | REMEDYREPACK INC. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA018279 |
Marketing Category: | NDA |
Start Marketing Date: | 20120921 |
Package NDC: | 52125-098-02 |
Package Description: | 30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (52125-098-02) |
NDC Code | 52125-098-02 |
Proprietary Name | Potassium Chloride |
Package Description | 30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (52125-098-02) |
Product NDC | 52125-098 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | POTASSIUM CHLORIDE |
Dosage Form Name | TABLET, EXTENDED RELEASE |
Route Name | ORAL |
Start Marketing Date | 20120921 |
Marketing Category Name | NDA |
Labeler Name | REMEDYREPACK INC. |
Substance Name | POTASSIUM CHLORIDE |
Strength Number | 750 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Potassium Compounds [Chemical/Ingredient],Potassium Salt [EPC] |