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Nostrilla
Nostrilla - 63736-072-01 - (Oxymetazoline Hydrochloride)
Drug Information of Nostrilla
| Product NDC: | 63736-072 |
| Proprietary Name: | Nostrilla |
| Non Proprietary Name: | Oxymetazoline Hydrochloride |
| Active Ingredient(s): | .0005 mL/100mL & nbsp; Oxymetazoline Hydrochloride |
| Administration Route(s): | NASAL |
| Dosage Form(s): | SPRAY, METERED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Nostrilla
| Product NDC: | 63736-072 |
| Labeler Name: | Insight Pharmaceuticals |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20090608 |
Package Information of Nostrilla
| Package NDC: | 63736-072-01 |
| Package Description: | 1 BOTTLE, SPRAY in 1 CARTON (63736-072-01) > 15 mL in 1 BOTTLE, SPRAY |
NDC Information of Nostrilla
| NDC Code | 63736-072-01 |
| Proprietary Name | Nostrilla |
| Package Description | 1 BOTTLE, SPRAY in 1 CARTON (63736-072-01) > 15 mL in 1 BOTTLE, SPRAY |
| Product NDC | 63736-072 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Oxymetazoline Hydrochloride |
| Dosage Form Name | SPRAY, METERED |
| Route Name | NASAL |
| Start Marketing Date | 20090608 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Insight Pharmaceuticals |
| Substance Name | OXYMETAZOLINE HYDROCHLORIDE |
| Strength Number | .0005 |
| Strength Unit | mL/100mL |
| Pharmaceutical Classes |
