Sodium Citrate and Citric Acid
- Product NDC
- 55154-9410
- 11-digit product format
- 551549410
- Labeler code
- 55154
- Product ID
- 55154-9410_4d547376-2495-4db1-8283-e3ed9d31df25
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- SODIUM CITRATE and CITRIC ACID MONOHYDRATE
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- Cardinal Health
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 1969-01-01
- Marketing end
- 2019-10-31
- Substance
- SODIUM CITRATE, UNSPECIFIED FORM; ANHYDROUS CITRIC ACID
- Active strength
- 500 mg/5mL; mg/5mL
- Pharmacologic classes
- Acidifying Activity [MoA],Calculi Dissolution Agent [EPC],Anti-coagulant [EPC],Decreased Coagulation Factor Activity [PE],Calcium Chelating Activity [MoA],Acidifying Activity [MoA],Calculi Dissolution Agent [EPC],Anti-coagulant [EPC],Decreased Coagulation Factor Activity [PE],Calcium Chelating Activity [MoA]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record