Betimol - 68669-522-05 - (timolol)

Alphabetical Index


Drug Information of Betimol

Product NDC: 68669-522
Proprietary Name: Betimol
Non Proprietary Name: timolol
Active Ingredient(s): 2.5    mg/mL & nbsp;   timolol
Administration Route(s): OPHTHALMIC
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Betimol

Product NDC: 68669-522
Labeler Name: Vistakon Pharmaceuticals LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020439
Marketing Category: NDA
Start Marketing Date: 20001001

Package Information of Betimol

Package NDC: 68669-522-05
Package Description: 5 mL in 1 BOTTLE (68669-522-05)

NDC Information of Betimol

NDC Code 68669-522-05
Proprietary Name Betimol
Package Description 5 mL in 1 BOTTLE (68669-522-05)
Product NDC 68669-522
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name timolol
Dosage Form Name SOLUTION
Route Name OPHTHALMIC
Start Marketing Date 20001001
Marketing Category Name NDA
Labeler Name Vistakon Pharmaceuticals LLC
Substance Name TIMOLOL
Strength Number 2.5
Strength Unit mg/mL
Pharmaceutical Classes

Complete Information of Betimol


General Information