Lisinopril - 0591-0407-30 - (Lisinopril)

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Drug Information of Lisinopril

Product NDC: 0591-0407
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: 0591-0407
Labeler Name: Watson Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076059
Marketing Category: ANDA
Start Marketing Date: 20020701

Package Information of Lisinopril

Package NDC: 0591-0407-30
Package Description: 30 TABLET in 1 BOTTLE, PLASTIC (0591-0407-30)

NDC Information of Lisinopril

NDC Code 0591-0407-30
Proprietary Name Lisinopril
Package Description 30 TABLET in 1 BOTTLE, PLASTIC (0591-0407-30)
Product NDC 0591-0407
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Lisinopril
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20020701
Marketing Category Name ANDA
Labeler Name Watson Laboratories, 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