Product NDC: | 65841-711 |
Proprietary Name: | OXYMETAZOLINE HYDROCHLORIDE |
Non Proprietary Name: | OXYMETAZOLINE HYDROCHLORIDE |
Active Ingredient(s): | .5 mg/mL & nbsp; OXYMETAZOLINE HYDROCHLORIDE |
Administration Route(s): | NASAL |
Dosage Form(s): | SPRAY, METERED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 65841-711 |
Labeler Name: | Cadila Healthcare Limited |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part341 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20090924 |
Package NDC: | 65841-711-07 |
Package Description: | 1 INHALER in 1 CARTON (65841-711-07) > 22 mL in 1 INHALER |
NDC Code | 65841-711-07 |
Proprietary Name | OXYMETAZOLINE HYDROCHLORIDE |
Package Description | 1 INHALER in 1 CARTON (65841-711-07) > 22 mL in 1 INHALER |
Product NDC | 65841-711 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | OXYMETAZOLINE HYDROCHLORIDE |
Dosage Form Name | SPRAY, METERED |
Route Name | NASAL |
Start Marketing Date | 20090924 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Cadila Healthcare Limited |
Substance Name | OXYMETAZOLINE HYDROCHLORIDE |
Strength Number | .5 |
Strength Unit | mg/mL |
Pharmaceutical Classes |