ACULAR - 16590-002-05 - (KETOROLAC TROMETHAMINE)

Alphabetical Index


Drug Information of ACULAR

Product NDC: 16590-002
Proprietary Name: ACULAR
Non Proprietary Name: KETOROLAC TROMETHAMINE
Active Ingredient(s): 5    mg/mL & nbsp;   KETOROLAC TROMETHAMINE
Administration Route(s): OPHTHALMIC
Dosage Form(s): SOLUTION/ DROPS
Coding System: National Drug Codes(NDC)

Labeler Information of ACULAR

Product NDC: 16590-002
Labeler Name: STAT Rx USA LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA019700
Marketing Category: NDA
Start Marketing Date: 19921201

Package Information of ACULAR

Package NDC: 16590-002-05
Package Description: 1 BOTTLE, DROPPER in 1 CARTON (16590-002-05) > 5 mL in 1 BOTTLE, DROPPER

NDC Information of ACULAR

NDC Code 16590-002-05
Proprietary Name ACULAR
Package Description 1 BOTTLE, DROPPER in 1 CARTON (16590-002-05) > 5 mL in 1 BOTTLE, DROPPER
Product NDC 16590-002
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name KETOROLAC TROMETHAMINE
Dosage Form Name SOLUTION/ DROPS
Route Name OPHTHALMIC
Start Marketing Date 19921201
Marketing Category Name NDA
Labeler Name STAT Rx USA LLC
Substance Name KETOROLAC TROMETHAMINE
Strength Number 5
Strength Unit mg/mL
Pharmaceutical Classes Cyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC]

Complete Information of ACULAR


General Information