Lisinopril - 43063-007-30 - (Lisinopril)

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Drug Information of Lisinopril

Product NDC: 43063-007
Proprietary Name: Lisinopril
Non Proprietary Name: Lisinopril
Active Ingredient(s): 20    mg/1 & nbsp;   Lisinopril
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Lisinopril

Product NDC: 43063-007
Labeler Name: PD-Rx Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077321
Marketing Category: ANDA
Start Marketing Date: 20060113

Package Information of Lisinopril

Package NDC: 43063-007-30
Package Description: 30 TABLET in 1 BOTTLE, PLASTIC (43063-007-30)

NDC Information of Lisinopril

NDC Code 43063-007-30
Proprietary Name Lisinopril
Package Description 30 TABLET in 1 BOTTLE, PLASTIC (43063-007-30)
Product NDC 43063-007
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Lisinopril
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20060113
Marketing Category Name ANDA
Labeler Name PD-Rx Pharmaceuticals, Inc.
Substance Name LISINOPRIL
Strength Number 20
Strength Unit mg/1
Pharmaceutical Classes Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA]

Complete Information of Lisinopril


General Information