SODIUM CHLORIDE
- Product NDC
- 51662-1522
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- SODIUM CHLORIDE
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- HF Acquisition Co LLC, DBA HealthFirst
- Application
- NDA016366
- Marketing category
- NDA
- Substance
- SODIUM CHLORIDE
- Current FDA listing
- Yes
Related Records
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|---|---|---|---|---|
| 51662-1522-1 | 500 mL in 1 BAG (51662-1522-1) | 2020-08-04 | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|---|---|---|---|
| 0.9% SODIUM CHLORIDE INJECTION, USP 500mL BAG | HF Acquisition Co LLC, DBA HealthFirst | 2020-08-04 | HUMAN PRESCRIPTION DRUG LABEL | 1 |