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ZESTRIL
ZESTRIL - 55289-106-30 - (Lisinopril)
Drug Information of ZESTRIL
| Product NDC: | 55289-106 |
| Proprietary Name: | ZESTRIL |
| Non Proprietary Name: | Lisinopril |
| Active Ingredient(s): | 20 mg/1 & nbsp; Lisinopril |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of ZESTRIL
| Product NDC: | 55289-106 |
| Labeler Name: | PD-Rx Pharmaceuticals, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA019777 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20111109 |
Package Information of ZESTRIL
| Package NDC: | 55289-106-30 |
| Package Description: | 30 TABLET in 1 BOTTLE, PLASTIC (55289-106-30) |
NDC Information of ZESTRIL
| NDC Code | 55289-106-30 |
| Proprietary Name | ZESTRIL |
| Package Description | 30 TABLET in 1 BOTTLE, PLASTIC (55289-106-30) |
| Product NDC | 55289-106 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Lisinopril |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20111109 |
| Marketing Category Name | NDA |
| Labeler Name | PD-Rx Pharmaceuticals, Inc. |
| Substance Name | LISINOPRIL |
| Strength Number | 20 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
