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Naphazoline
Naphazoline - 17478-216-12 - (Naphazoline Hydrochloride)
Drug Information of Naphazoline
| Product NDC: | 17478-216 |
| Proprietary Name: | Naphazoline |
| Non Proprietary Name: | Naphazoline Hydrochloride |
| Active Ingredient(s): | 1 mg/mL & nbsp; Naphazoline Hydrochloride |
| Administration Route(s): | OPHTHALMIC |
| Dosage Form(s): | SOLUTION/ DROPS |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Naphazoline
| Product NDC: | 17478-216 |
| Labeler Name: | Akorn, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA083590 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19951219 |
Package Information of Naphazoline
| Package NDC: | 17478-216-12 |
| Package Description: | 1 BOTTLE, DROPPER in 1 CARTON (17478-216-12) > 15 mL in 1 BOTTLE, DROPPER |
NDC Information of Naphazoline
| NDC Code | 17478-216-12 |
| Proprietary Name | Naphazoline |
| Package Description | 1 BOTTLE, DROPPER in 1 CARTON (17478-216-12) > 15 mL in 1 BOTTLE, DROPPER |
| Product NDC | 17478-216 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Naphazoline Hydrochloride |
| Dosage Form Name | SOLUTION/ DROPS |
| Route Name | OPHTHALMIC |
| Start Marketing Date | 19951219 |
| Marketing Category Name | ANDA |
| Labeler Name | Akorn, Inc. |
| Substance Name | NAPHAZOLINE HYDROCHLORIDE |
| Strength Number | 1 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |
