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Effer-K
Effer-K - 51801-013-30 - (POTASSIUM BICARBONATE)
Drug Information of Effer-K
| Product NDC: | 51801-013 |
| Proprietary Name: | Effer-K |
| Non Proprietary Name: | POTASSIUM BICARBONATE |
| Active Ingredient(s): | 391 mg/1 & nbsp; POTASSIUM BICARBONATE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, EFFERVESCENT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Effer-K
| Product NDC: | 51801-013 |
| Labeler Name: | Nomax Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20130130 |
Package Information of Effer-K
| Package NDC: | 51801-013-30 |
| Package Description: | 30 POUCH in 1 CARTON (51801-013-30) > 1 TABLET, EFFERVESCENT in 1 POUCH |
NDC Information of Effer-K
| NDC Code | 51801-013-30 |
| Proprietary Name | Effer-K |
| Package Description | 30 POUCH in 1 CARTON (51801-013-30) > 1 TABLET, EFFERVESCENT in 1 POUCH |
| Product NDC | 51801-013 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | POTASSIUM BICARBONATE |
| Dosage Form Name | TABLET, EFFERVESCENT |
| Route Name | ORAL |
| Start Marketing Date | 20130130 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Nomax Inc. |
| Substance Name | POTASSIUM BICARBONATE |
| Strength Number | 391 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Potassium Compounds [Chemical/Ingredient],Potassium Salt [EPC] |
