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Amiloride Hydrochloride and Hydrochlorothiazide
Amiloride Hydrochloride and Hydrochlorothiazide - 0555-0483-05 - (Amiloride Hydrochloride and Hydrochlorothiazide)
Drug Information of Amiloride Hydrochloride and Hydrochlorothiazide
| Product NDC: | 0555-0483 |
| Proprietary Name: | Amiloride Hydrochloride and Hydrochlorothiazide |
| Non Proprietary Name: | Amiloride Hydrochloride and Hydrochlorothiazide |
| Active Ingredient(s): | 5; 50 mg/1; mg/1 & nbsp; Amiloride Hydrochloride and Hydrochlorothiazide |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Amiloride Hydrochloride and Hydrochlorothiazide
| Product NDC: | 0555-0483 |
| Labeler Name: | Barr Laboratories Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA071111 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19891201 |
Package Information of Amiloride Hydrochloride and Hydrochlorothiazide
| Package NDC: | 0555-0483-05 |
| Package Description: | 1000 TABLET in 1 BOTTLE (0555-0483-05) |
NDC Information of Amiloride Hydrochloride and Hydrochlorothiazide
| NDC Code | 0555-0483-05 |
| Proprietary Name | Amiloride Hydrochloride and Hydrochlorothiazide |
| Package Description | 1000 TABLET in 1 BOTTLE (0555-0483-05) |
| Product NDC | 0555-0483 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Amiloride Hydrochloride and Hydrochlorothiazide |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 19891201 |
| Marketing Category Name | ANDA |
| Labeler Name | Barr Laboratories Inc. |
| Substance Name | AMILORIDE HYDROCHLORIDE; HYDROCHLOROTHIAZIDE |
| Strength Number | 5; 50 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes | Decreased Renal K+ Excretion [PE],Increased Diuresis [PE],Potassium-sparing Diuretic [EPC],Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient] |
