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IOPIDINE
IOPIDINE - 0065-0660-10 - (apraclonidine hydrochloride)
Drug Information of IOPIDINE
| Product NDC: | 0065-0660 |
| Proprietary Name: | IOPIDINE |
| Non Proprietary Name: | apraclonidine hydrochloride |
| Active Ingredient(s): | 10 mg/mL & nbsp; apraclonidine hydrochloride |
| Administration Route(s): | OPHTHALMIC |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of IOPIDINE
| Product NDC: | 0065-0660 |
| Labeler Name: | Alcon Laboratories, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA019779 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19880515 |
Package Information of IOPIDINE
| Package NDC: | 0065-0660-10 |
| Package Description: | .1 mL in 1 BOTTLE, PLASTIC (0065-0660-10) |
NDC Information of IOPIDINE
| NDC Code | 0065-0660-10 |
| Proprietary Name | IOPIDINE |
| Package Description | .1 mL in 1 BOTTLE, PLASTIC (0065-0660-10) |
| Product NDC | 0065-0660 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | apraclonidine hydrochloride |
| Dosage Form Name | SOLUTION |
| Route Name | OPHTHALMIC |
| Start Marketing Date | 19880515 |
| Marketing Category Name | NDA |
| Labeler Name | Alcon Laboratories, Inc. |
| Substance Name | APRACLONIDINE HYDROCHLORIDE |
| Strength Number | 10 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Adrenergic alpha-Agonists [MoA],alpha-Adrenergic Agonist [EPC] |
