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potassium chloride
potassium chloride - 76237-279-30 - (potassium chloride)
Drug Information of potassium chloride
| Product NDC: | 76237-279 |
| Proprietary Name: | potassium chloride |
| Non Proprietary Name: | potassium chloride |
| Active Ingredient(s): | 750 mg/1 & nbsp; potassium chloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of potassium chloride
| Product NDC: | 76237-279 |
| Labeler Name: | McKesson Contract Packaging |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA018238 |
| Marketing Category: | NDA AUTHORIZED GENERIC |
| Start Marketing Date: | 20130415 |
Package Information of potassium chloride
| Package NDC: | 76237-279-30 |
| Package Description: | 6 BLISTER PACK in 1 BOX, UNIT-DOSE (76237-279-30) > 5 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK |
NDC Information of potassium chloride
| NDC Code | 76237-279-30 |
| Proprietary Name | potassium chloride |
| Package Description | 6 BLISTER PACK in 1 BOX, UNIT-DOSE (76237-279-30) > 5 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK |
| Product NDC | 76237-279 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | potassium chloride |
| Dosage Form Name | CAPSULE, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20130415 |
| Marketing Category Name | NDA AUTHORIZED GENERIC |
| 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] |
