Product NDC: | 35356-948 |
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: | 35356-948 |
Labeler Name: | Lake Erie Medical DBA Quality Care Products LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA077321 |
Marketing Category: | ANDA |
Start Marketing Date: | 20070215 |
Package NDC: | 35356-948-60 |
Package Description: | 60 TABLET in 1 BOTTLE (35356-948-60) |
NDC Code | 35356-948-60 |
Proprietary Name | LISINOPRIL |
Package Description | 60 TABLET in 1 BOTTLE (35356-948-60) |
Product NDC | 35356-948 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | LISINOPRIL |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20070215 |
Marketing Category Name | ANDA |
Labeler Name | Lake Erie Medical DBA Quality Care Products LLC |
Substance Name | LISINOPRIL |
Strength Number | 40 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA] |