MAGNESIUM SULFATE
- Product NDC
- 51662-1372
- 11-digit product format
- 516621372
- Labeler code
- 51662
- Product ID
- 51662-1372_ef7bd6e6-d631-7e93-e053-2a95a90aef83
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- MAGNESIUM SULFATE
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- HF Acquisition Co LLC, DBA HealthFirst
- Application
- NDA019316
- Marketing category
- NDA
- Marketing start
- 2019-10-14
- Substance
- MAGNESIUM SULFATE HEPTAHYDRATE
- Active strength
- 500 mg/mL
- Pharmacologic classes
- 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 [MoA], Osmotic Laxative [EPC], Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- MAGNESIUM SULFATE
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| MAGNESIUM SULFATE HEPTAHYDRATE | 500 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | SK47B8698T |
| Rxcui | 1658236 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 51662-1372-1 | MAGNESIUM SULFATE | 20 mL in 1 VIAL, SINGLE-DOSE | INJECTION, SOLUTION | 20 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 51662-1372 | MAGNESIUM SULFATE INJECTION, SOLUTION [HF ACQUISITION CO LLC, DBA HEALTHFIRST] | 3 | Current NDC, Legacy NDC, 1 package rows | 20221211_94e9a33f-39c4-4bc5-e053-2a95a90a43ac.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 51662-1372-1 | 51662137201 | 20 mL in 1 VIAL, SINGLE-DOSE (51662-1372-1) | 20 ml | 2019-10-14 | 0000-00-00 | No | No | Current |