Product NDC: | 51477-002 |
Proprietary Name: | potassium chloride |
Non Proprietary Name: | potassium chloride |
Active Ingredient(s): | 600 mg/1 & nbsp; potassium chloride |
Administration Route(s): | ORAL |
Dosage Form(s): | CAPSULE, EXTENDED RELEASE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 51477-002 |
Labeler Name: | Nesher Pharmaceuticals (USA) LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA018238 |
Marketing Category: | NDA AUTHORIZED GENERIC |
Start Marketing Date: | 20101025 |
Package NDC: | 51477-002-04 |
Package Description: | 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (51477-002-04) |
NDC Code | 51477-002-04 |
Proprietary Name | potassium chloride |
Package Description | 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (51477-002-04) |
Product NDC | 51477-002 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | potassium chloride |
Dosage Form Name | CAPSULE, EXTENDED RELEASE |
Route Name | ORAL |
Start Marketing Date | 20101025 |
Marketing Category Name | NDA AUTHORIZED GENERIC |
Labeler Name | Nesher Pharmaceuticals (USA) LLC |
Substance Name | POTASSIUM CHLORIDE |
Strength Number | 600 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Potassium Compounds [Chemical/Ingredient],Potassium Salt [EPC] |