Sodium Chloride
- Product NDC
- 55154-3183
- 11-digit product format
- 551543183
- Labeler code
- 55154
- Product ID
- 55154-3183_32e206c0-426b-436e-8512-4dc4ee898764
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sodium Chloride
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Cardinal Health
- Application
- NDA018800
- Marketing category
- NDA
- Marketing start
- 1982-10-29
- Marketing end
- 0000-00-00
- Substance
- SODIUM CHLORIDE
- Active strength
- 9 mg/mL
- Pharmacologic classes
- Osmotic Laxativ
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- Current FDA listing
- Historical FDA.report record