Cambia

Product NDC
13913-011
11-digit product format
139130011
Labeler code
13913
Product ID
13913-011_90212a85-4b76-4a51-a22b-15016a491238
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
diclofenac potassium
Dosage form
POWDER, FOR SOLUTION
Route
ORAL
Labeler
Assertio Therapeutics, Inc.
Application
NDA022165
Marketing category
NDA
Marketing start
2010-04-20
Marketing end
0000-00-00
Substance
DICLOFENAC POTASSIUM
Active strength
50 mg/1
Pharmacologic classes
Cyclooxygenase Inhibitors [MoA],Decreased Prostaglandin Production [PE],Anti-Inflammatory Agents, Non-Steroidal [CS],Nonsteroidal Anti-inflammatory Drug [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
13913-011-01EA - Each13913-011d76a9591-d0ce-4730-9396-ca68d7af797312015-01-05
13913-011-19EA - Each13913-011076c2ac6-483a-46d5-80af-0d71ffc326e012015-01-05

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
13913-011-19139130011199 PACKET in 1 CARTON (13913-011-19) > 1 POWDER, FOR SOLUTION in 1 PACKET (13913-011-01) 9 packet2010-04-200000-00-00NoNoCurrent