Product NDC: | 0245-0043 |
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: | 0245-0043 |
Labeler Name: | Upsher-Smith Laboratories, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA019123 |
Marketing Category: | NDA |
Start Marketing Date: | 19860417 |
Package NDC: | 0245-0043-55 |
Package Description: | 1 BAG in 1 BOX (0245-0043-55) > 5000 TABLET, EXTENDED RELEASE in 1 BAG |
NDC Code | 0245-0043-55 |
Proprietary Name | Potassium Chloride |
Package Description | 1 BAG in 1 BOX (0245-0043-55) > 5000 TABLET, EXTENDED RELEASE in 1 BAG |
Product NDC | 0245-0043 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Potassium Chloride |
Dosage Form Name | TABLET, EXTENDED RELEASE |
Route Name | ORAL |
Start Marketing Date | 19860417 |
Marketing Category Name | NDA |
Labeler Name | Upsher-Smith Laboratories, Inc. |
Substance Name | POTASSIUM CHLORIDE |
Strength Number | 750 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Potassium Compounds [Chemical/Ingredient],Potassium Salt [EPC] |