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Triamterene and Hydrochlorothiazide
Triamterene and Hydrochlorothiazide - 51079-433-20 - (Triamterene and Hydrochlorothiazide)
Drug Information of Triamterene and Hydrochlorothiazide
| Product NDC: | 51079-433 |
| Proprietary Name: | Triamterene and Hydrochlorothiazide |
| Non Proprietary Name: | Triamterene and Hydrochlorothiazide |
| Active Ingredient(s): | 50; 75 mg/1; mg/1 & nbsp; Triamterene and Hydrochlorothiazide |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Triamterene and Hydrochlorothiazide
| Product NDC: | 51079-433 |
| Labeler Name: | UDL Laboratories, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA019129 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20110922 |
Package Information of Triamterene and Hydrochlorothiazide
| Package NDC: | 51079-433-20 |
| Package Description: | 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-433-20) > 1 TABLET in 1 BLISTER PACK (51079-433-01) |
NDC Information of Triamterene and Hydrochlorothiazide
| NDC Code | 51079-433-20 |
| Proprietary Name | Triamterene and Hydrochlorothiazide |
| Package Description | 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-433-20) > 1 TABLET in 1 BLISTER PACK (51079-433-01) |
| Product NDC | 51079-433 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Triamterene and Hydrochlorothiazide |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20110922 |
| Marketing Category Name | NDA |
| Labeler Name | UDL Laboratories, Inc. |
| Substance Name | HYDROCHLOROTHIAZIDE; TRIAMTERENE |
| Strength Number | 50; 75 |
| 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] |
