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NDC 00338-1708-40 Magnesium Sulfate 2 g/50mL Details
Magnesium Sulfate 2 g/50mL
Magnesium Sulfate is a INTRAVENOUS INJECTION, SOLUTION in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Baxter Healthcare Corporation. The primary component is MAGNESIUM SULFATE HEPTAHYDRATE.
Product Information
NDC | 00338-1708 |
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Product ID | 0338-1708_b5a8b04e-abe3-41fd-adb7-7f968118bf52 |
Associated GPIs | 79400010402040 |
GCN Sequence Number | 063340 |
GCN Sequence Number Description | magnesium sulfate in water PIGGYBACK 2 G/50 ML INTRAVEN |
HIC3 | C1H |
HIC3 Description | MAGNESIUM SALTS REPLACEMENT |
GCN | 99090 |
HICL Sequence Number | 039652 |
HICL Sequence Number Description | MAGNESIUM SULFATE IN STERILE WATER |
Brand/Generic | Generic |
Proprietary Name | Magnesium Sulfate |
Proprietary Name Suffix | n/a |
Non-Proprietary Name | Magnesium Sulfate Heptahydrate |
Product Type | HUMAN PRESCRIPTION DRUG |
Dosage Form | INJECTION, SOLUTION |
Route | INTRAVENOUS |
Active Ingredient Strength | 2 |
Active Ingredient Units | g/50mL |
Substance Name | MAGNESIUM SULFATE HEPTAHYDRATE |
Labeler Name | Baxter Healthcare Corporation |
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 | ANDA211966 |
Listing Certified Through | 2024-12-31 |
Package
NDC 00338-1708-40 (00338170840)
NDC Package Code | 0338-1708-40 |
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Billing NDC | 00338170840 |
Package | 40 BAG in 1 CARTON (0338-1708-40) / 50 mL in 1 BAG |
Marketing Start Date | 2020-06-01 |
NDC Exclude Flag | N |
Pricing Information | N/A |