Sodium Chloride
- Product NDC
- 55154-0103
- 11-digit product format
- 551540103
- Labeler code
- 55154
- Product ID
- 55154-0103_3afe4ee3-585e-423f-a5e9-939c60e80068
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sodium Chloride
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS
- Labeler
- Cardinal Health
- Application
- NDA018803
- Marketing category
- NDA
- Marketing start
- 2005-02-28
- Marketing end
- 2019-11-30
- Substance
- SODIUM CHLORIDE
- Active strength
- 9 mg/mL
- Pharmacologic classes
- Osmotic Laxative [EPC],Increased Large Intestinal Motility [PE],Inhibition Large Intestine Fluid/Electrolyte Absorption [PE],Osmotic Activity [MoA]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record