Ketoprofen

Product NDC
66267-126
11-digit product format
662670126
Labeler code
66267
Product ID
66267-126_9cbdfd9b-927b-533e-e053-2995a90a6fd9
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Ketoprofen
Dosage form
CAPSULE
Route
ORAL
Labeler
NuCare Pharmaceuticals, Inc.
Application
ANDA073517
Marketing category
ANDA
Marketing start
1993-01-01
Marketing end
0000-00-00
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
2021-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
66267-126-21EA - Each66267-126ae74ca31-aec6-4764-b148-dd4f73d295ae12016-11-08
66267-126-60EA - Each66267-1266f60a4af-1d95-4dfa-9de1-3dd1d6ff150e12016-11-08