ketorolac tromethamine

Product NDC
68071-3591
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
ketorolac tromethamine
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
NuCare Pharmaceuticals,Inc.
Application
ANDA217038
Marketing category
ANDA
Substance
KETOROLAC TROMETHAMINE
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
68071-3591-44 TABLET, FILM COATED in 1 BOTTLE (68071-3591-4) 2024-04-05NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Ketorolac Tromethamine Tablets USP, 10 mg Rx onlyNuCare Pharmaceuticals,Inc.2024-04-05HUMAN PRESCRIPTION DRUG LABEL1