Home
>
National Drug Code (NDC)
>
K-TAB
K-TAB - 53808-0277-1 - (POTASSIUM CHLORIDE)
Drug Information of K-TAB
| Product NDC: | 53808-0277 |
| Proprietary Name: | K-TAB |
| 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 K-TAB
| Product NDC: | 53808-0277 |
| Labeler Name: | State of Florida DOH Central Pharmacy |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA018279 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20090701 |
Package Information of K-TAB
| Package NDC: | 53808-0277-1 |
| Package Description: | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (53808-0277-1) |
NDC Information of K-TAB
| NDC Code | 53808-0277-1 |
| Proprietary Name | K-TAB |
| Package Description | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (53808-0277-1) |
| Product NDC | 53808-0277 |
| 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 | 20090701 |
| Marketing Category Name | NDA |
| Labeler Name | State of Florida DOH Central Pharmacy |
| Substance Name | POTASSIUM CHLORIDE |
| Strength Number | 750 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Potassium Compounds [Chemical/Ingredient],Potassium Salt [EPC] |
