Product NDC: | 52584-168 |
Proprietary Name: | Magnesium Sulfate |
Non Proprietary Name: | Magnesium Sulfate Heptahydrate |
Active Ingredient(s): | 500 mg/mL & nbsp; Magnesium Sulfate Heptahydrate |
Administration Route(s): | INTRAMUSCULAR; INTRAVENOUS |
Dosage Form(s): | INJECTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 52584-168 |
Labeler Name: | General Injectables & Vaccines, Inc |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED DRUG OTHER |
Start Marketing Date: | 20100901 |
Package NDC: | 52584-168-02 |
Package Description: | 1 VIAL, SINGLE-DOSE in 1 BAG (52584-168-02) > 20 mL in 1 VIAL, SINGLE-DOSE |
NDC Code | 52584-168-02 |
Proprietary Name | Magnesium Sulfate |
Package Description | 1 VIAL, SINGLE-DOSE in 1 BAG (52584-168-02) > 20 mL in 1 VIAL, SINGLE-DOSE |
Product NDC | 52584-168 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Magnesium Sulfate Heptahydrate |
Dosage Form Name | INJECTION |
Route Name | INTRAMUSCULAR; INTRAVENOUS |
Start Marketing Date | 20100901 |
Marketing Category Name | UNAPPROVED DRUG OTHER |
Labeler Name | General Injectables & Vaccines, Inc |
Substance Name | MAGNESIUM SULFATE HEPTAHYDRATE |
Strength Number | 500 |
Strength Unit | mg/mL |
Pharmaceutical Classes |