MIOSTAT - 0065-0023-15 - (carbachol)

Alphabetical Index


Drug Information of MIOSTAT

Product NDC: 0065-0023
Proprietary Name: MIOSTAT
Non Proprietary Name: carbachol
Active Ingredient(s): .1    mg/mL & nbsp;   carbachol
Administration Route(s): OPHTHALMIC
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of MIOSTAT

Product NDC: 0065-0023
Labeler Name: Alcon Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA016968
Marketing Category: NDA
Start Marketing Date: 19740415

Package Information of MIOSTAT

Package NDC: 0065-0023-15
Package Description: 12 VIAL, GLASS in 1 CARTON (0065-0023-15) > 1.5 mL in 1 VIAL, GLASS

NDC Information of MIOSTAT

NDC Code 0065-0023-15
Proprietary Name MIOSTAT
Package Description 12 VIAL, GLASS in 1 CARTON (0065-0023-15) > 1.5 mL in 1 VIAL, GLASS
Product NDC 0065-0023
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name carbachol
Dosage Form Name SOLUTION
Route Name OPHTHALMIC
Start Marketing Date 19740415
Marketing Category Name NDA
Labeler Name Alcon Laboratories, Inc.
Substance Name CARBACHOL
Strength Number .1
Strength Unit mg/mL
Pharmaceutical Classes

Complete Information of MIOSTAT


General Information