ReadySharp Ketorolac

Product NDC
68788-7439
11-digit product format
687887439
Labeler code
68788
Product ID
68788-7439_a6f3f72c-a66b-4581-a449-8b6727094ce7
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
KETOROLAC TROMETHAMINE
Dosage form
INJECTION, SOLUTION
Route
INTRAMUSCULAR; INTRAVENOUS
Labeler
Preferred Pharmaceuticals, Inc.
Application
ANDA074802
Marketing category
ANDA
Marketing start
1997-06-05
Marketing end
0000-00-00
Substance
KETOROLAC TROMETHAMINE
Active strength
15 mg/mL
Pharmacologic classes
Cyclooxygenase Inhibitors [MoA],Anti-Inflammatory Agents, Non-Steroidal [CS],Nonsteroidal Anti-inflammatory Drug [EPC],Cyclooxygenase Inhibitor [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
68788-7439-1EA - Each68788-7439beed6fd1-05e1-4b53-b984-d8d787faca3a12020-04-20