Lisinopril - 68788-9912-3 - (Lisinopril)

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Drug Information of Lisinopril

Product NDC: 68788-9912
Proprietary Name: Lisinopril
Non Proprietary Name: Lisinopril
Active Ingredient(s): 10    mg/1 & nbsp;   Lisinopril
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Lisinopril

Product NDC: 68788-9912
Labeler Name: Preferred Pharmaceuticals, Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076063
Marketing Category: ANDA
Start Marketing Date: 20120130

Package Information of Lisinopril

Package NDC: 68788-9912-3
Package Description: 30 TABLET in 1 BOTTLE, PLASTIC (68788-9912-3)

NDC Information of Lisinopril

NDC Code 68788-9912-3
Proprietary Name Lisinopril
Package Description 30 TABLET in 1 BOTTLE, PLASTIC (68788-9912-3)
Product NDC 68788-9912
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Lisinopril
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20120130
Marketing Category Name ANDA
Labeler Name Preferred Pharmaceuticals, Inc
Substance Name LISINOPRIL
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA]

Complete Information of Lisinopril


General Information