Product NDC: | 49873-044 |
Proprietary Name: | Sato Clear |
Non Proprietary Name: | NAPHAZOLINE HYDROCHLORIDE |
Active Ingredient(s): | 12 mg/100mL & nbsp; NAPHAZOLINE HYDROCHLORIDE |
Administration Route(s): | OPHTHALMIC |
Dosage Form(s): | SOLUTION/ DROPS |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 49873-044 |
Labeler Name: | Sato Pharmaceutical Co., Ltd. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part349 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 19890531 |
Package NDC: | 49873-044-01 |
Package Description: | 1 BOTTLE, PLASTIC in 1 CARTON (49873-044-01) > 15 mL in 1 BOTTLE, PLASTIC |
NDC Code | 49873-044-01 |
Proprietary Name | Sato Clear |
Package Description | 1 BOTTLE, PLASTIC in 1 CARTON (49873-044-01) > 15 mL in 1 BOTTLE, PLASTIC |
Product NDC | 49873-044 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | NAPHAZOLINE HYDROCHLORIDE |
Dosage Form Name | SOLUTION/ DROPS |
Route Name | OPHTHALMIC |
Start Marketing Date | 19890531 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Sato Pharmaceutical Co., Ltd. |
Substance Name | NAPHAZOLINE HYDROCHLORIDE |
Strength Number | 12 |
Strength Unit | mg/100mL |
Pharmaceutical Classes |