Home
>
National Drug Code (NDC)
>
Klor-Con M
Klor-Con M - 76237-194-30 - (Potassium Chloride)
Drug Information of Klor-Con M
| Product NDC: | 76237-194 |
| Proprietary Name: | Klor-Con M |
| 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) |
Labeler Information of Klor-Con M
| Product NDC: | 76237-194 |
| Labeler Name: | McKesson Contract Packaging |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA074726 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20111207 |
Package Information of Klor-Con M
| Package NDC: | 76237-194-30 |
| Package Description: | 6 BLISTER PACK in 1 BOX, UNIT-DOSE (76237-194-30) > 5 TABLET, EXTENDED RELEASE in 1 BLISTER PACK |
NDC Information of Klor-Con M
| NDC Code | 76237-194-30 |
| Proprietary Name | Klor-Con M |
| Package Description | 6 BLISTER PACK in 1 BOX, UNIT-DOSE (76237-194-30) > 5 TABLET, EXTENDED RELEASE in 1 BLISTER PACK |
| Product NDC | 76237-194 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Potassium Chloride |
| Dosage Form Name | TABLET, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20111207 |
| Marketing Category Name | ANDA |
| Labeler Name | McKesson Contract Packaging |
| Substance Name | POTASSIUM CHLORIDE |
| Strength Number | 750 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Potassium Compounds [Chemical/Ingredient],Potassium Salt [EPC] |
