ALAMAST - 68669-711-10 - (pemirolast potassium)

Alphabetical Index


Drug Information of ALAMAST

Product NDC: 68669-711
Proprietary Name: ALAMAST
Non Proprietary Name: pemirolast potassium
Active Ingredient(s): 1    mg/mL & nbsp;   pemirolast potassium
Administration Route(s): OPHTHALMIC
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of ALAMAST

Product NDC: 68669-711
Labeler Name: Vistakon Pharmaceuticals LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021079
Marketing Category: NDA
Start Marketing Date: 20000501

Package Information of ALAMAST

Package NDC: 68669-711-10
Package Description: 10 mL in 1 BOTTLE (68669-711-10)

NDC Information of ALAMAST

NDC Code 68669-711-10
Proprietary Name ALAMAST
Package Description 10 mL in 1 BOTTLE (68669-711-10)
Product NDC 68669-711
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name pemirolast potassium
Dosage Form Name SOLUTION
Route Name OPHTHALMIC
Start Marketing Date 20000501
Marketing Category Name NDA
Labeler Name Vistakon Pharmaceuticals LLC
Substance Name PEMIROLAST POTASSIUM
Strength Number 1
Strength Unit mg/mL
Pharmaceutical Classes Decreased Histamine Release [PE],Mast Cell Stabilizer [EPC]

Complete Information of ALAMAST


General Information