Product NDC: | 0615-1318 |
Proprietary Name: | Potassium Chloride |
Non Proprietary Name: | Potassium |
Active Ingredient(s): | 750 mg/1 & nbsp; Potassium |
Administration Route(s): | ORAL |
Dosage Form(s): | CAPSULE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0615-1318 |
Labeler Name: | NCS HealthCare of KY, Inc dba Vangard Labs |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA077419 |
Marketing Category: | ANDA |
Start Marketing Date: | 20080602 |
Package NDC: | 0615-1318-05 |
Package Description: | 15 CAPSULE in 1 BLISTER PACK (0615-1318-05) |
NDC Code | 0615-1318-05 |
Proprietary Name | Potassium Chloride |
Package Description | 15 CAPSULE in 1 BLISTER PACK (0615-1318-05) |
Product NDC | 0615-1318 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Potassium |
Dosage Form Name | CAPSULE |
Route Name | ORAL |
Start Marketing Date | 20080602 |
Marketing Category Name | ANDA |
Labeler Name | NCS HealthCare of KY, Inc dba Vangard Labs |
Substance Name | POTASSIUM CHLORIDE |
Strength Number | 750 |
Strength Unit | mg/1 |
Pharmaceutical Classes |