Lodine - 63629-1376-9 - (etodolac)

Alphabetical Index


Drug Information of Lodine

Product NDC: 63629-1376
Proprietary Name: Lodine
Non Proprietary Name: etodolac
Active Ingredient(s): 300    mg/1 & nbsp;   etodolac
Administration Route(s): ORAL
Dosage Form(s): CAPSULE, GELATIN COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Lodine

Product NDC: 63629-1376
Labeler Name: bryant ranch prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075126
Marketing Category: ANDA
Start Marketing Date: 20090630

Package Information of Lodine

Package NDC: 63629-1376-9
Package Description: 21 CAPSULE, GELATIN COATED in 1 BOTTLE (63629-1376-9)

NDC Information of Lodine

NDC Code 63629-1376-9
Proprietary Name Lodine
Package Description 21 CAPSULE, GELATIN COATED in 1 BOTTLE (63629-1376-9)
Product NDC 63629-1376
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name etodolac
Dosage Form Name CAPSULE, GELATIN COATED
Route Name ORAL
Start Marketing Date 20090630
Marketing Category Name ANDA
Labeler Name bryant ranch prepack
Substance Name ETODOLAC
Strength Number 300
Strength Unit mg/1
Pharmaceutical Classes Cyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC]

Complete Information of Lodine


General Information