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Oxymetazoline Hydrochloride
Oxymetazoline Hydrochloride - 64762-865-22 - (Oxymetazoline Hydrochloride)
Drug Information of Oxymetazoline Hydrochloride
| Product NDC: | 64762-865 |
| Proprietary Name: | Oxymetazoline Hydrochloride |
| Non Proprietary Name: | Oxymetazoline Hydrochloride |
| Active Ingredient(s): | .2 mg/.4mL & nbsp; Oxymetazoline Hydrochloride |
| Administration Route(s): | NASAL |
| Dosage Form(s): | SPRAY, METERED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Oxymetazoline Hydrochloride
| Product NDC: | 64762-865 |
| Labeler Name: | Dynamic Pharmaceuticals |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20091104 |
Package Information of Oxymetazoline Hydrochloride
| Package NDC: | 64762-865-22 |
| Package Description: | 1 BOTTLE, PUMP in 1 CARTON (64762-865-22) > 22 mL in 1 BOTTLE, PUMP |
NDC Information of Oxymetazoline Hydrochloride
| NDC Code | 64762-865-22 |
| Proprietary Name | Oxymetazoline Hydrochloride |
| Package Description | 1 BOTTLE, PUMP in 1 CARTON (64762-865-22) > 22 mL in 1 BOTTLE, PUMP |
| Product NDC | 64762-865 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Oxymetazoline Hydrochloride |
| Dosage Form Name | SPRAY, METERED |
| Route Name | NASAL |
| Start Marketing Date | 20091104 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Dynamic Pharmaceuticals |
| Substance Name | OXYMETAZOLINE HYDROCHLORIDE |
| Strength Number | .2 |
| Strength Unit | mg/.4mL |
| Pharmaceutical Classes |
