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urocit-k
urocit-k - 0178-0615-01 - (potassium citrate)
Drug Information of urocit-k
| Product NDC: | 0178-0615 |
| 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: | 0178-0615 |
| Labeler Name: | Mission Pharmacal Company |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA019071 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20100127 |
Package Information of urocit-k
| Package NDC: | 0178-0615-01 |
| Package Description: | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (0178-0615-01) |
NDC Information of urocit-k
| NDC Code | 0178-0615-01 |
| Proprietary Name | urocit-k |
| Package Description | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (0178-0615-01) |
| Product NDC | 0178-0615 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | potassium citrate |
| Dosage Form Name | TABLET, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20100127 |
| Marketing Category Name | NDA |
| Labeler Name | Mission Pharmacal Company |
| Substance Name | POTASSIUM CITRATE |
| Strength Number | 15 |
| Strength Unit | meq/1 |
| Pharmaceutical Classes | Potassium Compounds [Chemical/Ingredient],Potassium Salt [EPC] |
