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Apraclonidine Ophthalmic
Apraclonidine Ophthalmic - 17478-716-11 - (Apraclonidine Hydrochloride)
Drug Information of Apraclonidine Ophthalmic
| Product NDC: | 17478-716 |
| Proprietary Name: | Apraclonidine Ophthalmic |
| Non Proprietary Name: | Apraclonidine Hydrochloride |
| Active Ingredient(s): | 5 mg/mL & nbsp; Apraclonidine Hydrochloride |
| Administration Route(s): | OPHTHALMIC |
| Dosage Form(s): | SOLUTION/ DROPS |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Apraclonidine Ophthalmic
| Product NDC: | 17478-716 |
| Labeler Name: | Akorn Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA077764 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20090812 |
Package Information of Apraclonidine Ophthalmic
| Package NDC: | 17478-716-11 |
| Package Description: | 1 BOTTLE, DROPPER in 1 CARTON (17478-716-11) > 10 mL in 1 BOTTLE, DROPPER |
NDC Information of Apraclonidine Ophthalmic
| NDC Code | 17478-716-11 |
| Proprietary Name | Apraclonidine Ophthalmic |
| Package Description | 1 BOTTLE, DROPPER in 1 CARTON (17478-716-11) > 10 mL in 1 BOTTLE, DROPPER |
| Product NDC | 17478-716 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Apraclonidine Hydrochloride |
| Dosage Form Name | SOLUTION/ DROPS |
| Route Name | OPHTHALMIC |
| Start Marketing Date | 20090812 |
| Marketing Category Name | ANDA |
| Labeler Name | Akorn Inc. |
| Substance Name | APRACLONIDINE HYDROCHLORIDE |
| Strength Number | 5 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Adrenergic alpha-Agonists [MoA],alpha-Adrenergic Agonist [EPC] |
