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Privine
Privine - 63736-662-02 - (Naphazoline Hydrochloride)
Drug Information of Privine
| Product NDC: | 63736-662 |
| Proprietary Name: | Privine |
| Non Proprietary Name: | Naphazoline Hydrochloride |
| Active Ingredient(s): | .1 mL/20mL & nbsp; Naphazoline Hydrochloride |
| Administration Route(s): | NASAL |
| Dosage Form(s): | SPRAY |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Privine
| Product NDC: | 63736-662 |
| Labeler Name: | Insight Pharmaceuticals |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20090716 |
Package Information of Privine
| Package NDC: | 63736-662-02 |
| Package Description: | 1 BOTTLE in 1 BOX (63736-662-02) > 20 mL in 1 BOTTLE |
NDC Information of Privine
| NDC Code | 63736-662-02 |
| Proprietary Name | Privine |
| Package Description | 1 BOTTLE in 1 BOX (63736-662-02) > 20 mL in 1 BOTTLE |
| Product NDC | 63736-662 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Naphazoline Hydrochloride |
| Dosage Form Name | SPRAY |
| Route Name | NASAL |
| Start Marketing Date | 20090716 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Insight Pharmaceuticals |
| Substance Name | NAPHAZOLINE HYDROCHLORIDE |
| Strength Number | .1 |
| Strength Unit | mL/20mL |
| Pharmaceutical Classes |
