FDA NDC Directory · JSON-LD · Markdown
NDC 0409-2168 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION
| Generic name | MAGNESIUM SULFATE |
|---|---|
| Labeler / Manufacturer | Hospira, Inc. |
| Marketing category | Abbreviated NDA (generic) · App ANDA202411 |
| Dosage form / route | INJECTION, SOLUTION · INTRAMUSCULAR INTRAVENOUS |
| Active ingredients | MAGNESIUM SULFATE HEPTAHYDRATE (500 mg/mL) |
| Marketing started | 20050331 |
| Package count | 1 |
Source: openFDA. Public-domain (CC0).