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Sodium Chloride Hypertonicity
Sodium Chloride Hypertonicity - 0904-5315-38 - (sodium chloride)
Drug Information of Sodium Chloride Hypertonicity
| Product NDC: | 0904-5315 |
| Proprietary Name: | Sodium Chloride Hypertonicity |
| Non Proprietary Name: | sodium chloride |
| Active Ingredient(s): | 50 mg/g & nbsp; sodium chloride |
| Administration Route(s): | OPHTHALMIC |
| Dosage Form(s): | OINTMENT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Sodium Chloride Hypertonicity
| Product NDC: | 0904-5315 |
| Labeler Name: | Major Pharmaceuticals |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part349 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20110101 |
Package Information of Sodium Chloride Hypertonicity
| Package NDC: | 0904-5315-38 |
| Package Description: | 3.5 g in 1 TUBE (0904-5315-38) |
NDC Information of Sodium Chloride Hypertonicity
| NDC Code | 0904-5315-38 |
| Proprietary Name | Sodium Chloride Hypertonicity |
| Package Description | 3.5 g in 1 TUBE (0904-5315-38) |
| Product NDC | 0904-5315 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | sodium chloride |
| Dosage Form Name | OINTMENT |
| 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/g |
| Pharmaceutical Classes |
