NDC | 53157-798-60 |
Set ID | 1a2ad203-63fe-42ac-88c6-23dd28385005 |
Category | HUMAN PRESCRIPTION DRUG LABEL |
Packager | Haemonetics Manufacturing Inc |
Generic Name | |
Product Class | Anti-coagulant |
Product Number | |
Application Number | NDA760305 |
- DESCRIPTION
- INDICATIONS AND USAGE
- CONTRAINDICATIONS
- WARNINGS
- PRECAUTIONS
- HOW SUPPLIED
- PACKAGE/LABEL PRINCIPAL DISPLAY PANEL
- References
-
INGREDIENTS AND APPEARANCE
SODIUM CITRATE
anticoagulant sodium citrate solution solutionProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:53157-798 Route of Administration INTRAVENOUS DEA Schedule CII Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SODIUM CITRATE (UNII: 1Q73Q2JULR) (ANHYDROUS CITRIC ACID - UNII:XF417D3PSL) SODIUM CITRATE 10.0 g in 250 mL Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:53157-798-60 36 in 1 CARTON 1 250 mL in 1 BAG; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date NDA NDA760305 06/30/1978 Labeler - Haemonetics Manufacturing Inc (078598396) Registrant - Haemonetics Manufacturing Inc (078598396) Establishment Name Address ID/FEI Business Operations Haemonetics Manufacturing Inc 078598396 MANUFACTURE(53157-798) , STERILIZE(53157-798) , LABEL(53157-798)