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Lisinopril and Hydrochlorothiazide
Lisinopril and Hydrochlorothiazide - 51079-698-40 - (lisinopril and hydrochlorothiazide)
Drug Information of Lisinopril and Hydrochlorothiazide
| Product NDC: | 51079-698 |
| Proprietary Name: | Lisinopril and Hydrochlorothiazide |
| Non Proprietary Name: | lisinopril and hydrochlorothiazide |
| Active Ingredient(s): | 12.5; 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: | 51079-698 |
| Labeler Name: | UDL Laboratories, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA076113 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20100608 |
Package Information of Lisinopril and Hydrochlorothiazide
| Package NDC: | 51079-698-40 |
| Package Description: | 100 TABLET in 1 BOTTLE, PLASTIC (51079-698-40) |
NDC Information of Lisinopril and Hydrochlorothiazide
| NDC Code | 51079-698-40 |
| Proprietary Name | Lisinopril and Hydrochlorothiazide |
| Package Description | 100 TABLET in 1 BOTTLE, PLASTIC (51079-698-40) |
| Product NDC | 51079-698 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | lisinopril and hydrochlorothiazide |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20100608 |
| Marketing Category Name | ANDA |
| Labeler Name | UDL Laboratories, Inc. |
| Substance Name | HYDROCHLOROTHIAZIDE; LISINOPRIL |
| Strength Number | 12.5; 20 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes | Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient] |
