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Naphazoline Hydrochloride and Pheniramine Maleate
Naphazoline Hydrochloride and Pheniramine Maleate - 17478-065-12 - (Naphazoline Hydrochloride and Pheniramine Maleate)
Drug Information of Naphazoline Hydrochloride and Pheniramine Maleate
| Product NDC: | 17478-065 |
| Proprietary Name: | Naphazoline Hydrochloride and Pheniramine Maleate |
| Non Proprietary Name: | Naphazoline Hydrochloride and Pheniramine Maleate |
| Active Ingredient(s): | .25; 3 mg/mL; mg/mL & nbsp; Naphazoline Hydrochloride and Pheniramine Maleate |
| Administration Route(s): | OPHTHALMIC |
| Dosage Form(s): | SOLUTION/ DROPS |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Naphazoline Hydrochloride and Pheniramine Maleate
| Product NDC: | 17478-065 |
| Labeler Name: | Akorn, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA202795 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20130124 |
Package Information of Naphazoline Hydrochloride and Pheniramine Maleate
| Package NDC: | 17478-065-12 |
| Package Description: | 1 BOTTLE, DROPPER in 1 CARTON (17478-065-12) > 15 mL in 1 BOTTLE, DROPPER |
NDC Information of Naphazoline Hydrochloride and Pheniramine Maleate
| NDC Code | 17478-065-12 |
| Proprietary Name | Naphazoline Hydrochloride and Pheniramine Maleate |
| Package Description | 1 BOTTLE, DROPPER in 1 CARTON (17478-065-12) > 15 mL in 1 BOTTLE, DROPPER |
| Product NDC | 17478-065 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Naphazoline Hydrochloride and Pheniramine Maleate |
| Dosage Form Name | SOLUTION/ DROPS |
| Route Name | OPHTHALMIC |
| Start Marketing Date | 20130124 |
| Marketing Category Name | ANDA |
| Labeler Name | Akorn, Inc. |
| Substance Name | NAPHAZOLINE HYDROCHLORIDE; PHENIRAMINE MALEATE |
| Strength Number | .25; 3 |
| Strength Unit | mg/mL; mg/mL |
| Pharmaceutical Classes |
