Product NDC: | 0904-5314 |
Proprietary Name: | Sodium Chloride Hypertonicity |
Non Proprietary Name: | sodium chloride |
Active Ingredient(s): | 50 mg/mL & nbsp; sodium chloride |
Administration Route(s): | OPHTHALMIC |
Dosage Form(s): | SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0904-5314 |
Labeler Name: | Major Pharmaceuticals |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part349 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20110101 |
Package NDC: | 0904-5314-35 |
Package Description: | 1 BOTTLE in 1 CARTON (0904-5314-35) > 15 mL in 1 BOTTLE |
NDC Code | 0904-5314-35 |
Proprietary Name | Sodium Chloride Hypertonicity |
Package Description | 1 BOTTLE in 1 CARTON (0904-5314-35) > 15 mL in 1 BOTTLE |
Product NDC | 0904-5314 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | sodium chloride |
Dosage Form Name | SOLUTION |
Route Name | OPHTHALMIC |
Start Marketing Date | 20110101 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Major Pharmaceuticals |
Substance Name | SODIUM CHLORIDE |
Strength Number | 50 |
Strength Unit | mg/mL |
Pharmaceutical Classes |