Product NDC: | 60760-266 |
Proprietary Name: | LISINOPRIL |
Non Proprietary Name: | LISINOPRIL |
Active Ingredient(s): | 5 mg/1 & nbsp; LISINOPRIL |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 60760-266 |
Labeler Name: | St Marys Medical Park Pharmacy |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA075743 |
Marketing Category: | ANDA |
Start Marketing Date: | 20130516 |
Package NDC: | 60760-266-30 |
Package Description: | 30 TABLET in 1 BOTTLE, PLASTIC (60760-266-30) |
NDC Code | 60760-266-30 |
Proprietary Name | LISINOPRIL |
Package Description | 30 TABLET in 1 BOTTLE, PLASTIC (60760-266-30) |
Product NDC | 60760-266 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | LISINOPRIL |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20130516 |
Marketing Category Name | ANDA |
Labeler Name | St Marys Medical Park Pharmacy |
Substance Name | LISINOPRIL |
Strength Number | 5 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA] |