Product NDC: | 64679-942 |
Proprietary Name: | Lisinopril |
Non Proprietary Name: | Lisinopril |
Active Ingredient(s): | 40 mg/1 & nbsp; Lisinopril |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 64679-942 |
Labeler Name: | Wockhardt USA LLC. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA078402 |
Marketing Category: | ANDA |
Start Marketing Date: | 20070419 |
Package NDC: | 64679-942-05 |
Package Description: | 500 TABLET in 1 BOTTLE (64679-942-05) |
NDC Code | 64679-942-05 |
Proprietary Name | Lisinopril |
Package Description | 500 TABLET in 1 BOTTLE (64679-942-05) |
Product NDC | 64679-942 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Lisinopril |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20070419 |
Marketing Category Name | ANDA |
Labeler Name | Wockhardt USA LLC. |
Substance Name | LISINOPRIL |
Strength Number | 40 |
Strength Unit | mg/1 |
Pharmaceutical Classes |