ZESTRIL - 0310-0133-11 - (Lisinopril)

Alphabetical Index


Drug Information of ZESTRIL

Product NDC: 0310-0133
Proprietary Name: ZESTRIL
Non Proprietary Name: Lisinopril
Active Ingredient(s): 30    mg/1 & nbsp;   Lisinopril
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of ZESTRIL

Product NDC: 0310-0133
Labeler Name: AstraZeneca Pharmaceuticals LP
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA019777
Marketing Category: NDA
Start Marketing Date: 20100922

Package Information of ZESTRIL

Package NDC: 0310-0133-11
Package Description: 100 TABLET in 1 BOTTLE (0310-0133-11)

NDC Information of ZESTRIL

NDC Code 0310-0133-11
Proprietary Name ZESTRIL
Package Description 100 TABLET in 1 BOTTLE (0310-0133-11)
Product NDC 0310-0133
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Lisinopril
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20100922
Marketing Category Name NDA
Labeler Name AstraZeneca Pharmaceuticals LP
Substance Name LISINOPRIL
Strength Number 30
Strength Unit mg/1
Pharmaceutical Classes Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA]

Complete Information of ZESTRIL


General Information