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Apraclonidine
Apraclonidine - 61314-665-10 - (Apraclonidine)
Drug Information of Apraclonidine
| Product NDC: | 61314-665 |
| Proprietary Name: | Apraclonidine |
| Non Proprietary Name: | Apraclonidine |
| Active Ingredient(s): | 5.75 mg/mL & nbsp; Apraclonidine |
| Administration Route(s): | OPHTHALMIC |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Apraclonidine
| Product NDC: | 61314-665 |
| Labeler Name: | Falcon Pharmaceuticals, Ltd. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020258 |
| Marketing Category: | NDA AUTHORIZED GENERIC |
| Start Marketing Date: | 20090719 |
Package Information of Apraclonidine
| Package NDC: | 61314-665-10 |
| Package Description: | 10 mL in 1 BOTTLE (61314-665-10) |
NDC Information of Apraclonidine
| NDC Code | 61314-665-10 |
| Proprietary Name | Apraclonidine |
| Package Description | 10 mL in 1 BOTTLE (61314-665-10) |
| Product NDC | 61314-665 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Apraclonidine |
| Dosage Form Name | SOLUTION |
| Route Name | OPHTHALMIC |
| Start Marketing Date | 20090719 |
| Marketing Category Name | NDA AUTHORIZED GENERIC |
| Labeler Name | Falcon Pharmaceuticals, Ltd. |
| Substance Name | APRACLONIDINE HYDROCHLORIDE |
| Strength Number | 5.75 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Adrenergic alpha-Agonists [MoA],alpha-Adrenergic Agonist [EPC] |
