NDC 51662-1468
MANNITOL
Mannitol
MANNITOL is a Intravenous Injection, Solution in the Human Prescription Drug category. It is labeled and distributed by Hf Acquisition Co Llc, Dba Healthfirst. The primary component is Mannitol.
Product ID | 51662-1468_999ce711-2d5c-0d7d-e053-2995a90a2689 |
NDC | 51662-1468 |
Product Type | Human Prescription Drug |
Proprietary Name | MANNITOL |
Generic Name | Mannitol |
Dosage Form | Injection, Solution |
Route of Administration | INTRAVENOUS |
Marketing Start Date | 2019-12-13 |
Marketing Category | NDA / NDA |
Application Number | NDA016269 |
Labeler Name | HF Acquisition Co LLC, DBA HealthFirst |
Substance Name | MANNITOL |
Active Ingredient Strength | 13 g/50mL |
Pharm Classes | Increased Diuresis [PE],Osmotic Activity [MoA],Osmotic Diuretic [EPC] |
NDC Exclude Flag | N |
Listing Certified Through | 2020-12-31 |