Lisinopril - 63304-535-77 - (Lisinopril)

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Drug Information of Lisinopril

Product NDC: 63304-535
Proprietary Name: Lisinopril
Non Proprietary Name: Lisinopril
Active Ingredient(s): 40    mg/1 & nbsp;   Lisinopril
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Lisinopril

Product NDC: 63304-535
Labeler Name: Ranbaxy Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075944
Marketing Category: ANDA
Start Marketing Date: 20020702

Package Information of Lisinopril

Package NDC: 63304-535-77
Package Description: 10 BLISTER PACK in 1 CARTON (63304-535-77) > 10 TABLET in 1 BLISTER PACK (63304-535-11)

NDC Information of Lisinopril

NDC Code 63304-535-77
Proprietary Name Lisinopril
Package Description 10 BLISTER PACK in 1 CARTON (63304-535-77) > 10 TABLET in 1 BLISTER PACK (63304-535-11)
Product NDC 63304-535
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Lisinopril
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20020702
Marketing Category Name ANDA
Labeler Name Ranbaxy Pharmaceuticals Inc.
Substance Name LISINOPRIL
Strength Number 40
Strength Unit mg/1
Pharmaceutical Classes Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA]

Complete Information of Lisinopril


General Information