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K-Tab
K-Tab - 0074-7804-13 - (Potassium Chloride)
Drug Information of K-Tab
| Product NDC: | 0074-7804 |
| 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: | 0074-7804 |
| Labeler Name: | AbbVie Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA018279 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19800609 |
Package Information of K-Tab
| Package NDC: | 0074-7804-13 |
| Package Description: | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0074-7804-13) |
NDC Information of K-Tab
| NDC Code | 0074-7804-13 |
| Proprietary Name | K-Tab |
| Package Description | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0074-7804-13) |
| Product NDC | 0074-7804 |
| 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 | 19800609 |
| Marketing Category Name | NDA |
| Labeler Name | AbbVie Inc. |
| Substance Name | POTASSIUM CHLORIDE |
| Strength Number | 750 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Potassium Compounds [Chemical/Ingredient],Potassium Salt [EPC] |
