LOVAZA - 21695-795-72 - (omega-3-acid ethyl esters)

Alphabetical Index


Drug Information of LOVAZA

Product NDC: 21695-795
Proprietary Name: LOVAZA
Non Proprietary Name: omega-3-acid ethyl esters
Active Ingredient(s): 1    g/1 & nbsp;   omega-3-acid ethyl esters
Administration Route(s): ORAL
Dosage Form(s): CAPSULE, LIQUID FILLED
Coding System: National Drug Codes(NDC)

Labeler Information of LOVAZA

Product NDC: 21695-795
Labeler Name: Rebel Distributors Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021654
Marketing Category: NDA
Start Marketing Date: 20081021

Package Information of LOVAZA

Package NDC: 21695-795-72
Package Description: 120 CAPSULE, LIQUID FILLED in 1 BOTTLE (21695-795-72)

NDC Information of LOVAZA

NDC Code 21695-795-72
Proprietary Name LOVAZA
Package Description 120 CAPSULE, LIQUID FILLED in 1 BOTTLE (21695-795-72)
Product NDC 21695-795
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name omega-3-acid ethyl esters
Dosage Form Name CAPSULE, LIQUID FILLED
Route Name ORAL
Start Marketing Date 20081021
Marketing Category Name NDA
Labeler Name Rebel Distributors Corp
Substance Name OMEGA-3-ACID ETHYL ESTERS
Strength Number 1
Strength Unit g/1
Pharmaceutical Classes

Complete Information of LOVAZA


General Information