Product NDC: | 0065-0397 |
Proprietary Name: | Cyclogyl |
Non Proprietary Name: | cyclopentolate hydrochloride |
Active Ingredient(s): | 20 mg/mL & nbsp; cyclopentolate hydrochloride |
Administration Route(s): | OPHTHALMIC |
Dosage Form(s): | SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0065-0397 |
Labeler Name: | Alcon Laboratories, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA084108 |
Marketing Category: | ANDA |
Start Marketing Date: | 19751015 |
Package NDC: | 0065-0397-15 |
Package Description: | 15 mL in 1 BOTTLE, PLASTIC (0065-0397-15) |
NDC Code | 0065-0397-15 |
Proprietary Name | Cyclogyl |
Package Description | 15 mL in 1 BOTTLE, PLASTIC (0065-0397-15) |
Product NDC | 0065-0397 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | cyclopentolate hydrochloride |
Dosage Form Name | SOLUTION |
Route Name | OPHTHALMIC |
Start Marketing Date | 19751015 |
Marketing Category Name | ANDA |
Labeler Name | Alcon Laboratories, Inc. |
Substance Name | CYCLOPENTOLATE HYDROCHLORIDE |
Strength Number | 20 |
Strength Unit | mg/mL |
Pharmaceutical Classes |