Luvira

Product NDC
69336-351
11-digit product format
693360351
Labeler code
69336
Product ID
69336-351_99d7525d-b62e-7f8e-e053-2a95a90a2080
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Luvira
Dosage form
CAPSULE
Route
ORAL
Labeler
Sterling-Knight Pharmaceuticals, LLC
Marketing category
UNAPPROVED DRUG OTHER
Marketing start
2019-11-07
Marketing end
0000-00-00
Substance
OMEGA-3-ACID ETHYL ESTERS; 12-HYDROXYEICOSAPENTAENOIC ACID, (12R)-; 4,7,10,13,16,19-DOCOSAHEXAENOIC ACID, (4E,7E,10E,13E,16E,19E)-
Active strength
1220 mg/1; mg/1; mg/1
Pharmacologic classes
Fatty Acids, Omega-3 [CS],Omega-3 Fatty Acid [EPC]
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
69336-351-90EA - Each69336-351f50778a1-ea97-47f4-b1ee-e5b483a0790012019-12-10