Product NDC: | 37205-753 |
Proprietary Name: | Saline Refills |
Non Proprietary Name: | SODIUM BICARBONATE, SODIUM CHLORIDE |
Active Ingredient(s): | 2300; 700 mg/1; mg/1 & nbsp; SODIUM BICARBONATE, SODIUM CHLORIDE |
Administration Route(s): | ORAL |
Dosage Form(s): | POWDER, FOR SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 37205-753 |
Labeler Name: | Cardinal Health 414, LLC |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED DRUG OTHER |
Start Marketing Date: | 20130401 |
Package NDC: | 37205-753-78 |
Package Description: | 100 PACKET in 1 CARTON (37205-753-78) > 1 POWDER, FOR SOLUTION in 1 PACKET |
NDC Code | 37205-753-78 |
Proprietary Name | Saline Refills |
Package Description | 100 PACKET in 1 CARTON (37205-753-78) > 1 POWDER, FOR SOLUTION in 1 PACKET |
Product NDC | 37205-753 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | SODIUM BICARBONATE, SODIUM CHLORIDE |
Dosage Form Name | POWDER, FOR SOLUTION |
Route Name | ORAL |
Start Marketing Date | 20130401 |
Marketing Category Name | UNAPPROVED DRUG OTHER |
Labeler Name | Cardinal Health 414, LLC |
Substance Name | SODIUM BICARBONATE; SODIUM CHLORIDE |
Strength Number | 2300; 700 |
Strength Unit | mg/1; mg/1 |
Pharmaceutical Classes |