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AMILORIDE HYDROCHLORIDE
AMILORIDE HYDROCHLORIDE - 54868-5214-3 - (amiloride hydrochloride)
Drug Information of AMILORIDE HYDROCHLORIDE
| Product NDC: | 54868-5214 |
| Proprietary Name: | AMILORIDE HYDROCHLORIDE |
| Non Proprietary Name: | amiloride hydrochloride |
| Active Ingredient(s): | 5 mg/1 & nbsp; amiloride hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of AMILORIDE HYDROCHLORIDE
| Product NDC: | 54868-5214 |
| Labeler Name: | Physicians Total Care, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA018200 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20050128 |
Package Information of AMILORIDE HYDROCHLORIDE
| Package NDC: | 54868-5214-3 |
| Package Description: | 10 TABLET in 1 BOTTLE, PLASTIC (54868-5214-3) |
NDC Information of AMILORIDE HYDROCHLORIDE
| NDC Code | 54868-5214-3 |
| Proprietary Name | AMILORIDE HYDROCHLORIDE |
| Package Description | 10 TABLET in 1 BOTTLE, PLASTIC (54868-5214-3) |
| Product NDC | 54868-5214 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | amiloride hydrochloride |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20050128 |
| Marketing Category Name | NDA |
| Labeler Name | Physicians Total Care, Inc. |
| Substance Name | AMILORIDE HYDROCHLORIDE |
| Strength Number | 5 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Decreased Renal K+ Excretion [PE],Increased Diuresis [PE],Potassium-sparing Diuretic [EPC] |
