NDC 51662-1359
0.9% SODIUM CHLORIDE
0.9% Sodium Chloride
0.9% SODIUM CHLORIDE is a Intramuscular; Intravenous; Subcutaneous Injection, Solution in the Human Prescription Drug category. It is labeled and distributed by Hf Acquisition Co Llc, Dba Healthfirst. The primary component is Sodium Chloride.
| Product ID | 51662-1359_8dfb05c0-77e9-2fa1-e053-2a95a90a3d33 |
| NDC | 51662-1359 |
| Product Type | Human Prescription Drug |
| Proprietary Name | 0.9% SODIUM CHLORIDE |
| Generic Name | 0.9% Sodium Chloride |
| Dosage Form | Injection, Solution |
| Route of Administration | INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS |
| Marketing Start Date | 2019-07-18 |
| Marketing Category | NDA / NDA |
| Application Number | NDA018803 |
| Labeler Name | HF Acquisition Co LLC, DBA HealthFirst |
| Substance Name | SODIUM CHLORIDE |
| Active Ingredient Strength | 9 mg/mL |
| Pharm Classes | Osmotic Laxative [EPC],Increased Large Intestinal Motility [PE],Inhibition Large Intestine Fluid/Electrolyte Absorption [PE],Osmotic Activity [MoA] |
| NDC Exclude Flag | N |
| Listing Certified Through | 2020-12-31 |