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OXYMETAZOLINE HYDROCHLORIDE
OXYMETAZOLINE HYDROCHLORIDE - 21695-875-30 - (OXYMETAZOLINE HYDROCHLORIDE)
Drug Information of OXYMETAZOLINE HYDROCHLORIDE
| Product NDC: | 21695-875 |
| 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) |
Labeler Information of OXYMETAZOLINE HYDROCHLORIDE
| Product NDC: | 21695-875 |
| Labeler Name: | Rebel Distributors Corp |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20081211 |
Package Information of OXYMETAZOLINE HYDROCHLORIDE
| Package NDC: | 21695-875-30 |
| Package Description: | 30 mL in 1 BOTTLE, SPRAY (21695-875-30) |
NDC Information of OXYMETAZOLINE HYDROCHLORIDE
| NDC Code | 21695-875-30 |
| Proprietary Name | OXYMETAZOLINE HYDROCHLORIDE |
| Package Description | 30 mL in 1 BOTTLE, SPRAY (21695-875-30) |
| Product NDC | 21695-875 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | OXYMETAZOLINE HYDROCHLORIDE |
| Dosage Form Name | SPRAY, METERED |
| Route Name | NASAL |
| Start Marketing Date | 20081211 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Rebel Distributors Corp |
| Substance Name | OXYMETAZOLINE HYDROCHLORIDE |
| Strength Number | .5 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |
