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UROCIT-K
UROCIT-K - 54868-6176-0 - (potassium citrate)
Drug Information of UROCIT-K
| Product NDC: | 54868-6176 |
| Proprietary Name: | UROCIT-K |
| Non Proprietary Name: | potassium citrate |
| Active Ingredient(s): | 15 meq/1 & nbsp; potassium citrate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of UROCIT-K
| Product NDC: | 54868-6176 |
| Labeler Name: | Physicians Total Care, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA019071 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20100915 |
Package Information of UROCIT-K
| Package NDC: | 54868-6176-0 |
| Package Description: | 10 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (54868-6176-0) |
NDC Information of UROCIT-K
| NDC Code | 54868-6176-0 |
| Proprietary Name | UROCIT-K |
| Package Description | 10 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (54868-6176-0) |
| Product NDC | 54868-6176 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | potassium citrate |
| Dosage Form Name | TABLET, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20100915 |
| Marketing Category Name | NDA |
| Labeler Name | Physicians Total Care, Inc. |
| Substance Name | POTASSIUM CITRATE |
| Strength Number | 15 |
| Strength Unit | meq/1 |
| Pharmaceutical Classes | Potassium Compounds [Chemical/Ingredient],Potassium Salt [EPC] |
