ACULAR - 21695-463-05 - (KETOROLAC TROMETHAMINE)

Alphabetical Index


Drug Information of ACULAR

Product NDC: 21695-463
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
Coding System: National Drug Codes(NDC)

Labeler Information of ACULAR

Product NDC: 21695-463
Labeler Name: Rebel Distributors Corp.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA019700
Marketing Category: NDA
Start Marketing Date: 19921109

Package Information of ACULAR

Package NDC: 21695-463-05
Package Description: 5 mL in 1 BOTTLE (21695-463-05)

NDC Information of ACULAR

NDC Code 21695-463-05
Proprietary Name ACULAR
Package Description 5 mL in 1 BOTTLE (21695-463-05)
Product NDC 21695-463
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name KETOROLAC TROMETHAMINE
Dosage Form Name SOLUTION
Route Name OPHTHALMIC
Start Marketing Date 19921109
Marketing Category Name NDA
Labeler Name Rebel Distributors Corp.
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