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SinuFrin
SinuFrin - 13709-231-07 - (Oxymetazoline Hydrochloride)
Drug Information of SinuFrin
| Product NDC: | 13709-231 |
| Proprietary Name: | SinuFrin |
| Non Proprietary Name: | Oxymetazoline Hydrochloride |
| Active Ingredient(s): | 7.5 mg/15mL & nbsp; Oxymetazoline Hydrochloride |
| Administration Route(s): | NASAL |
| Dosage Form(s): | SPRAY |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of SinuFrin
| Product NDC: | 13709-231 |
| Labeler Name: | NeilMed Pharmaceuticals Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20120715 |
Package Information of SinuFrin
| Package NDC: | 13709-231-07 |
| Package Description: | 15 mL in 1 BOTTLE (13709-231-07) |
NDC Information of SinuFrin
| NDC Code | 13709-231-07 |
| Proprietary Name | SinuFrin |
| Package Description | 15 mL in 1 BOTTLE (13709-231-07) |
| Product NDC | 13709-231 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Oxymetazoline Hydrochloride |
| Dosage Form Name | SPRAY |
| Route Name | NASAL |
| Start Marketing Date | 20120715 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | NeilMed Pharmaceuticals Inc |
| Substance Name | OXYMETAZOLINE HYDROCHLORIDE |
| Strength Number | 7.5 |
| Strength Unit | mg/15mL |
| Pharmaceutical Classes |
