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OXYMETAZOLINE HYDROCHLORIDE
OXYMETAZOLINE HYDROCHLORIDE - 68382-418-07 - (OXYMETAZOLINE HYDROCHLORIDE)
Drug Information of OXYMETAZOLINE HYDROCHLORIDE
| Product NDC: | 68382-418 |
| 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: | 68382-418 |
| Labeler Name: | Zydus Pharmaceuticals (USA) Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20090924 |
Package Information of OXYMETAZOLINE HYDROCHLORIDE
| Package NDC: | 68382-418-07 |
| Package Description: | 1 INHALER in 1 CARTON (68382-418-07) > 22 mL in 1 INHALER |
NDC Information of OXYMETAZOLINE HYDROCHLORIDE
| NDC Code | 68382-418-07 |
| Proprietary Name | OXYMETAZOLINE HYDROCHLORIDE |
| Package Description | 1 INHALER in 1 CARTON (68382-418-07) > 22 mL in 1 INHALER |
| Product NDC | 68382-418 |
| 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 | Zydus Pharmaceuticals (USA) Inc. |
| Substance Name | OXYMETAZOLINE HYDROCHLORIDE |
| Strength Number | .5 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |
