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POTASSIUM CHLORIDE
POTASSIUM CHLORIDE - 60760-601-30 - (POTASSIUM CHLORIDE)
Drug Information of POTASSIUM CHLORIDE
| Product NDC: | 60760-601 |
| Proprietary Name: | POTASSIUM CHLORIDE |
| Non Proprietary Name: | POTASSIUM CHLORIDE |
| Active Ingredient(s): | 20 meq/1 & nbsp; POTASSIUM CHLORIDE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of POTASSIUM CHLORIDE
| Product NDC: | 60760-601 |
| Labeler Name: | St Marys Medical Park Pharmacy . |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA076368 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20130516 |
Package Information of POTASSIUM CHLORIDE
| Package NDC: | 60760-601-30 |
| Package Description: | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (60760-601-30) |
NDC Information of POTASSIUM CHLORIDE
| NDC Code | 60760-601-30 |
| Proprietary Name | POTASSIUM CHLORIDE |
| Package Description | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (60760-601-30) |
| Product NDC | 60760-601 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | POTASSIUM CHLORIDE |
| Dosage Form Name | TABLET, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20130516 |
| Marketing Category Name | ANDA |
| Labeler Name | St Marys Medical Park Pharmacy . |
| Substance Name | POTASSIUM CHLORIDE |
| Strength Number | 20 |
| Strength Unit | meq/1 |
| Pharmaceutical Classes | Potassium Compounds [Chemical/Ingredient],Potassium Salt [EPC] |
