Ketorolac Tromethamine

Product NDC
67296-2171
11-digit product format
672962171
Labeler code
67296
Product ID
67296-2171_3b0ad5fe-5943-a868-e063-6294a90aa786
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Ketorolac Tromethamine
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Redpharm Drug
Application
ANDA216759
Marketing category
ANDA
Marketing start
2023-03-10
Substance
KETOROLAC TROMETHAMINE
Active strength
10 mg/1
Pharmacologic classes
Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitor [EPC], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
4EVE5946BQKETOROLAC TROMETHAMINE74103-07-4KETOROLAC TROMETHAMINE

Packages

Package NDC11-digit formatDescriptionMarketing startSampleExclude flagStatus
67296-2171-16729621710120 TABLET, FILM COATED in 1 BOTTLE (67296-2171-1) 2023-03-10NoNoHistorical
67296-2171-26729621710210 TABLET, FILM COATED in 1 BOTTLE (67296-2171-2) 2023-03-10NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Ketorolac Tromethamine Tablets, USP Rx onlyRedpharm Drug2025-07-29HUMAN PRESCRIPTION DRUG LABEL1