Product NDC: | 52584-966 |
Proprietary Name: | Bacteriastatic Sodium Chloride |
Non Proprietary Name: | Sodium Chloride |
Active Ingredient(s): | 9 mg/mL & nbsp; Sodium Chloride |
Administration Route(s): | INTRAVENOUS |
Dosage Form(s): | INJECTION, SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 52584-966 |
Labeler Name: | General Injectables & Vaccines, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA018800 |
Marketing Category: | NDA |
Start Marketing Date: | 20100601 |
Package NDC: | 52584-966-07 |
Package Description: | 1 VIAL, MULTI-DOSE in 1 BAG (52584-966-07) > 30 mL in 1 VIAL, MULTI-DOSE |
NDC Code | 52584-966-07 |
Proprietary Name | Bacteriastatic Sodium Chloride |
Package Description | 1 VIAL, MULTI-DOSE in 1 BAG (52584-966-07) > 30 mL in 1 VIAL, MULTI-DOSE |
Product NDC | 52584-966 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Sodium Chloride |
Dosage Form Name | INJECTION, SOLUTION |
Route Name | INTRAVENOUS |
Start Marketing Date | 20100601 |
Marketing Category Name | NDA |
Labeler Name | General Injectables & Vaccines, Inc. |
Substance Name | SODIUM CHLORIDE |
Strength Number | 9 |
Strength Unit | mg/mL |
Pharmaceutical Classes |