Product NDC: | 68788-9155 |
Proprietary Name: | Nasal |
Non Proprietary Name: | Oxymetazoline Hydrochloride |
Active Ingredient(s): | 5 g/100mL & nbsp; Oxymetazoline Hydrochloride |
Administration Route(s): | NASAL |
Dosage Form(s): | SPRAY |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 68788-9155 |
Labeler Name: | Preferred Pharmaceuticals, Inc |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part341 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20090317 |
Package NDC: | 68788-9155-3 |
Package Description: | 30 mL in 1 BOTTLE, SPRAY (68788-9155-3) |
NDC Code | 68788-9155-3 |
Proprietary Name | Nasal |
Package Description | 30 mL in 1 BOTTLE, SPRAY (68788-9155-3) |
Product NDC | 68788-9155 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Oxymetazoline Hydrochloride |
Dosage Form Name | SPRAY |
Route Name | NASAL |
Start Marketing Date | 20090317 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Preferred Pharmaceuticals, Inc |
Substance Name | OXYMETAZOLINE HYDROCHLORIDE |
Strength Number | 5 |
Strength Unit | g/100mL |
Pharmaceutical Classes |