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