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Potassium Chloride
Potassium Chloride - 62037-999-05 - (potassium chloride)
Drug Information of Potassium Chloride
| Product NDC: | 62037-999 |
| 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: | 62037-999 |
| Labeler Name: | Watson Pharma, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA076368 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20040818 |
Package Information of Potassium Chloride
| Package NDC: | 62037-999-05 |
| Package Description: | 500 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (62037-999-05) |
NDC Information of Potassium Chloride
| NDC Code | 62037-999-05 |
| Proprietary Name | Potassium Chloride |
| Package Description | 500 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (62037-999-05) |
| Product NDC | 62037-999 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | potassium chloride |
| Dosage Form Name | TABLET, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20040818 |
| Marketing Category Name | ANDA |
| Labeler Name | Watson Pharma, Inc. |
| Substance Name | POTASSIUM CHLORIDE |
| Strength Number | 20 |
| Strength Unit | meq/1 |
| Pharmaceutical Classes | Potassium Compounds [Chemical/Ingredient],Potassium Salt [EPC] |
