Acular - 0023-2181-05 - (Ketorolac Tromethamine)

Alphabetical Index


Drug Information of Acular

Product NDC: 0023-2181
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: 0023-2181
Labeler Name: Allergan, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA019700
Marketing Category: NDA
Start Marketing Date: 19921201

Package Information of Acular

Package NDC: 0023-2181-05
Package Description: 1 BOTTLE, DROPPER in 1 CARTON (0023-2181-05) > 5 mL in 1 BOTTLE, DROPPER

NDC Information of Acular

NDC Code 0023-2181-05
Proprietary Name Acular
Package Description 1 BOTTLE, DROPPER in 1 CARTON (0023-2181-05) > 5 mL in 1 BOTTLE, DROPPER
Product NDC 0023-2181
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 Allergan, Inc.
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