MANNITOL 12.5 g/50mL
MANNITOL · INJECTION, SOLUTION · HF Acquisition Co LLC, DBA HealthFirst
No Recall History
Plain English
MANNITOL is a injection, solution containing mannitol at 12.5 g/50mL, taken intravenous. Manufactured by HF Acquisition Co LLC, DBA HealthFirst.
Key Facts
- Brand Name
- MANNITOL
- Generic Name
- MANNITOL
- NDC Code (Product)
51662-1468- Manufacturer
- HF Acquisition Co LLC, DBA HealthFirst
- Strength
- 12.5 g/50mL
- Dosage Form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Marketing Status
- Application #
- NDA016269
- Drug Class
- Osmotic Diuretic [EPC]
- Marketing Start
- 12/13/2019
Recall History
No Recall HistoryFrequently Asked Questions
What is MANNITOL used for?
MANNITOL contains MANNITOL. It is a injection, solution taken intravenous. Consult your doctor for specific uses.
Is MANNITOL a controlled substance?
MANNITOL is not classified as a controlled substance by the DEA.
What is the generic name for MANNITOL?
The generic name for MANNITOL is MANNITOL. There are 9 other brand versions of MANNITOL.
What is the NDC code for MANNITOL 12.5 g/50mL?
The NDC (National Drug Code) for MANNITOL 12.5 g/50mL is 51662-1468, listed by HF Acquisition Co LLC, DBA HealthFirst.