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NDC 00409-1754-10 Magnesium Sulfate 500 mg/mL Details
Magnesium Sulfate 500 mg/mL
Magnesium Sulfate is a INTRAMUSCULAR; INTRAVENOUS INJECTION, SOLUTION in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Hospira, Inc.. The primary component is MAGNESIUM SULFATE HEPTAHYDRATE.
Product Information
| NDC | 00409-1754 |
|---|---|
| Product ID | 0409-1754_c4b61b4d-095a-4878-bb38-130efb1926c4 |
| Associated GPIs | 79400010402020 |
| GCN Sequence Number | 001413 |
| GCN Sequence Number Description | magnesium sulfate SYRINGE 500 MG/ML INJECTION |
| HIC3 | C1H |
| HIC3 Description | MAGNESIUM SALTS REPLACEMENT |
| GCN | 04120 |
| HICL Sequence Number | 000610 |
| HICL Sequence Number Description | MAGNESIUM SULFATE |
| Brand/Generic | Generic |
| Proprietary Name | Magnesium Sulfate |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | magnesium sulfate |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | INJECTION, SOLUTION |
| Route | INTRAMUSCULAR; INTRAVENOUS |
| Active Ingredient Strength | 500 |
| Active Ingredient Units | mg/mL |
| Substance Name | MAGNESIUM SULFATE HEPTAHYDRATE |
| Labeler Name | Hospira, Inc. |
| Pharmaceutical Class | Calculi Dissolution Agent [EPC], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Small Intestine Fluid/Electrolyte Absorption [PE], Magnesium Ion Exchange Activity [MoA], Osmotic Activity |
| DEA Schedule | n/a |
| Marketing Category | ANDA |
| Application Number | ANDA075151 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 00409-1754-10 (00409175410)
| NDC Package Code | 0409-1754-10 |
|---|---|
| Billing NDC | 00409175410 |
| Package | 10 CARTON in 1 PACKAGE (0409-1754-10) / 1 SYRINGE, PLASTIC in 1 CARTON / 10 mL in 1 SYRINGE, PLASTIC (0409-1754-15) |
| Marketing Start Date | 2006-11-28 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |