ketoprofen

Product NDC
23155-022
11-digit product format
231550022
Labeler code
23155
Product ID
23155-022_d298ce92-b8cb-4bd0-a71e-ff5378f2af14
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
ketoprofen
Dosage form
CAPSULE
Route
ORAL
Labeler
Heritage Pharma Labs Inc. d/b/a Avet Pharmaceuticals Labs Inc.
Application
ANDA074014
Marketing category
ANDA
Marketing start
2020-01-28
Marketing end
2022-03-31
Substance
KETOPROFEN
Active strength
75 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
0000-00-00
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
23155-022-01EA - Each23155-02243b9f36d-887b-4b53-985d-9494b5c34d8312020-04-20

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
23155-022-0123155002201100 CAPSULE in 1 BOTTLE (23155-022-01) 100 capsule2020-01-280000-00-00NoNoCurrent
23155-022-0523155002205500 CAPSULE in 1 BOTTLE (23155-022-05) 500 capsule2020-01-280000-00-00NoNoCurrent