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Nazal
Nazal - 49873-057-01 - (Naphazoline hydrochloride)
Drug Information of Nazal
| Product NDC: | 49873-057 |
| Proprietary Name: | Nazal |
| Non Proprietary Name: | Naphazoline hydrochloride |
| Active Ingredient(s): | 50 mg/100mL & nbsp; Naphazoline hydrochloride |
| Administration Route(s): | NASAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Nazal
| Product NDC: | 49873-057 |
| Labeler Name: | Sato Pharmaceutical Co., Ltd. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 19900611 |
Package Information of Nazal
| Package NDC: | 49873-057-01 |
| Package Description: | 1 BOTTLE in 1 CARTON (49873-057-01) > 30 mL in 1 BOTTLE |
NDC Information of Nazal
| NDC Code | 49873-057-01 |
| Proprietary Name | Nazal |
| Package Description | 1 BOTTLE in 1 CARTON (49873-057-01) > 30 mL in 1 BOTTLE |
| Product NDC | 49873-057 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Naphazoline hydrochloride |
| Dosage Form Name | LIQUID |
| Route Name | NASAL |
| Start Marketing Date | 19900611 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Sato Pharmaceutical Co., Ltd. |
| Substance Name | NAPHAZOLINE HYDROCHLORIDE |
| Strength Number | 50 |
| Strength Unit | mg/100mL |
| Pharmaceutical Classes |
