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Aqua Maris Isotonised
Aqua Maris Isotonised - 76260-101-30 - (Sodium chloride)
Drug Information of Aqua Maris Isotonised
| Product NDC: | 76260-101 |
| Proprietary Name: | Aqua Maris Isotonised |
| Non Proprietary Name: | Sodium chloride |
| Active Ingredient(s): | 11.25 mg/mL & nbsp; Sodium chloride |
| Administration Route(s): | NASAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Aqua Maris Isotonised
| Product NDC: | 76260-101 |
| Labeler Name: | JGL North America LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20011228 |
Package Information of Aqua Maris Isotonised
| Package NDC: | 76260-101-30 |
| Package Description: | 1 BOTTLE, SPRAY in 1 CARTON (76260-101-30) > 30 mL in 1 BOTTLE, SPRAY |
NDC Information of Aqua Maris Isotonised
| NDC Code | 76260-101-30 |
| Proprietary Name | Aqua Maris Isotonised |
| Package Description | 1 BOTTLE, SPRAY in 1 CARTON (76260-101-30) > 30 mL in 1 BOTTLE, SPRAY |
| Product NDC | 76260-101 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Sodium chloride |
| Dosage Form Name | LIQUID |
| Route Name | NASAL |
| Start Marketing Date | 20011228 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | JGL North America LLC |
| Substance Name | SODIUM CHLORIDE |
| Strength Number | 11.25 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |
