Product NDC: | 63736-663 |
Proprietary Name: | Privine |
Non Proprietary Name: | Naphazoline Hydrochloride |
Active Ingredient(s): | .125 mL/25mL & nbsp; Naphazoline Hydrochloride |
Administration Route(s): | NASAL |
Dosage Form(s): | SUSPENSION/ DROPS |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 63736-663 |
Labeler Name: | Insight Pharmaceuticals LLC |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part341 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20090716 |
Package NDC: | 63736-663-01 |
Package Description: | 1 BOTTLE in 1 BOX (63736-663-01) > 25 mL in 1 BOTTLE |
NDC Code | 63736-663-01 |
Proprietary Name | Privine |
Package Description | 1 BOTTLE in 1 BOX (63736-663-01) > 25 mL in 1 BOTTLE |
Product NDC | 63736-663 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Naphazoline Hydrochloride |
Dosage Form Name | SUSPENSION/ DROPS |
Route Name | NASAL |
Start Marketing Date | 20090716 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Insight Pharmaceuticals LLC |
Substance Name | NAPHAZOLINE HYDROCHLORIDE |
Strength Number | .125 |
Strength Unit | mL/25mL |
Pharmaceutical Classes |