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Sodium Chloride
Sodium Chloride - 17478-622-35 - (Sodium Chloride)
Drug Information of Sodium Chloride
| Product NDC: | 17478-622 |
| Proprietary Name: | Sodium Chloride |
| 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
| Product NDC: | 17478-622 |
| Labeler Name: | Akorn, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part349 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20060508 |
Package Information of Sodium Chloride
| Package NDC: | 17478-622-35 |
| Package Description: | 1 TUBE in 1 CARTON (17478-622-35) > 3.5 g in 1 TUBE |
NDC Information of Sodium Chloride
| NDC Code | 17478-622-35 |
| Proprietary Name | Sodium Chloride |
| Package Description | 1 TUBE in 1 CARTON (17478-622-35) > 3.5 g in 1 TUBE |
| Product NDC | 17478-622 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Sodium Chloride |
| Dosage Form Name | OINTMENT |
| Route Name | OPHTHALMIC |
| Start Marketing Date | 20060508 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Akorn, Inc. |
| Substance Name | SODIUM CHLORIDE |
| Strength Number | 50 |
| Strength Unit | mg/g |
| Pharmaceutical Classes |
