Etodolac

Product NDC
50090-1316
11-digit product format
500901316
Labeler code
50090
Product ID
50090-1316_d8755afb-5caa-4f61-b021-a718d13f1f8e
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Etodolac
Dosage form
TABLET, EXTENDED RELEASE
Route
ORAL
Labeler
A-S Medication Solutions
Application
ANDA076174
Marketing category
ANDA
Marketing start
2003-03-13
Marketing end
0000-00-00
Substance
ETODOLAC
Active strength
600 mg/1
Pharmacologic classes
Cyclooxygenase Inhibitors [MoA],Anti-Inflammatory Agents, Non-Steroidal [CS],Nonsteroidal Anti-inflammatory Drug [EPC]
NDC exclude flag
No
Listing certified through
2019-12-31
Current FDA listing
Historical FDA.report record

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
2M36281008ETODOLAC41340-25-4ETODOLAC