Etodolac

Product NDC
68788-9410
11-digit product format
687889410
Labeler code
68788
Product ID
68788-9410_334c0a22-9e9c-4bf6-9697-cb35c05e83cd
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Etodolac
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Preferred Pharmaceuticals Inc.
Application
ANDA076004
Marketing category
ANDA
Marketing start
2015-08-18
Marketing end
0000-00-00
Substance
ETODOLAC
Active strength
400 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
2021-12-31
Current FDA listing
Historical FDA.report record

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
68788-9410-168788941001100 TABLET, FILM COATED in 1 BOTTLE (68788-9410-1) 2015-08-180000-00-00NoNoCurrent
68788-9410-26878894100220 TABLET, FILM COATED in 1 BOTTLE (68788-9410-2) 2015-08-180000-00-00NoNoCurrent
68788-9410-36878894100330 TABLET, FILM COATED in 1 BOTTLE (68788-9410-3) 2015-08-180000-00-00NoNoCurrent
68788-9410-66878894100660 TABLET, FILM COATED in 1 BOTTLE (68788-9410-6) 2015-08-180000-00-00NoNoCurrent
68788-9410-96878894100990 TABLET, FILM COATED in 1 BOTTLE (68788-9410-9) 2015-08-180000-00-00NoNoCurrent