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Sodium Chloride
Sodium Chloride - 0487-9301-33 - (ISodium Chloride)
Drug Information of Sodium Chloride
| Product NDC: | 0487-9301 |
| Proprietary Name: | Sodium Chloride |
| Non Proprietary Name: | ISodium Chloride |
| Active Ingredient(s): | .027 mg/3mL & nbsp; ISodium Chloride |
| Administration Route(s): | RESPIRATORY (INHALATION) |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Sodium Chloride
| Product NDC: | 0487-9301 |
| Labeler Name: | Nephron Pharmaceuticals Corporation |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20020718 |
Package Information of Sodium Chloride
| Package NDC: | 0487-9301-33 |
| Package Description: | 30 POUCH in 1 CARTON (0487-9301-33) > 1 VIAL, SINGLE-USE in 1 POUCH > 3 mL in 1 VIAL, SINGLE-USE |
NDC Information of Sodium Chloride
| NDC Code | 0487-9301-33 |
| Proprietary Name | Sodium Chloride |
| Package Description | 30 POUCH in 1 CARTON (0487-9301-33) > 1 VIAL, SINGLE-USE in 1 POUCH > 3 mL in 1 VIAL, SINGLE-USE |
| Product NDC | 0487-9301 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | ISodium Chloride |
| Dosage Form Name | SOLUTION |
| Route Name | RESPIRATORY (INHALATION) |
| Start Marketing Date | 20020718 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Nephron Pharmaceuticals Corporation |
| Substance Name | SODIUM CHLORIDE |
| Strength Number | .027 |
| Strength Unit | mg/3mL |
| Pharmaceutical Classes |
