Home
>
National Drug Code (NDC)
>
Lisinopril and Hydrochlorothiazide
Lisinopril and Hydrochlorothiazide - 43063-130-90 - (Lisinopril and Hydrochlorothiazide)
Drug Information of Lisinopril and Hydrochlorothiazide
| Product NDC: | 43063-130 |
| Proprietary Name: | Lisinopril and Hydrochlorothiazide |
| Non Proprietary Name: | Lisinopril and Hydrochlorothiazide |
| Active Ingredient(s): | 25; 20 mg/1; mg/1 & nbsp; Lisinopril and Hydrochlorothiazide |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Lisinopril and Hydrochlorothiazide
| Product NDC: | 43063-130 |
| Labeler Name: | PD-Rx Pharmaceuticals, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA075776 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20100804 |
Package Information of Lisinopril and Hydrochlorothiazide
| Package NDC: | 43063-130-90 |
| Package Description: | 90 TABLET in 1 BOTTLE, PLASTIC (43063-130-90) |
NDC Information of Lisinopril and Hydrochlorothiazide
| NDC Code | 43063-130-90 |
| Proprietary Name | Lisinopril and Hydrochlorothiazide |
| Package Description | 90 TABLET in 1 BOTTLE, PLASTIC (43063-130-90) |
| Product NDC | 43063-130 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Lisinopril and Hydrochlorothiazide |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20100804 |
| Marketing Category Name | ANDA |
| Labeler Name | PD-Rx Pharmaceuticals, Inc. |
| Substance Name | HYDROCHLOROTHIAZIDE; LISINOPRIL |
| Strength Number | 25; 20 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes | Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient] |
