elliotts b

Generic: sodium cation, sodium bicarbonate, anhydrous dextrose, magnesium sulfate, potassium chloride, calcium chloride, sodium phosphate

Labeler: lukare medical, llc
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name elliotts b
Generic Name sodium cation, sodium bicarbonate, anhydrous dextrose, magnesium sulfate, potassium chloride, calcium chloride, sodium phosphate
Labeler lukare medical, llc
Dosage Form INJECTION
Routes
INTRATHECAL
Active Ingredients

anhydrous dextrose 8 mg/10mL, calcium chloride 2 mg/10mL, magnesium sulfate, unspecified form 3 mg/10mL, potassium chloride 3 mg/10mL, sodium bicarbonate 19 mg/10mL, sodium chloride 73 mg/10mL, sodium phosphate 2 mg/10mL

Manufacturer
Lukare Medical, LLC

Identifiers & Regulatory

Product NDC 55792-007
Product ID 55792-007_4a638cd1-6922-477a-aa17-a70865ae0bd8
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA020577
Listing Expiration 2026-12-31
Marketing Start 2013-06-04

Pharmacologic Class

Classes
alkalinizing activity [moa] blood coagulation factor [epc] calcium [cs] calculi dissolution agent [epc] cations divalent [cs] increased coagulation factor activity [pe] increased large intestinal motility [pe] inhibition large intestine fluid/electrolyte absorption [pe] inhibition small intestine fluid/electrolyte absorption [pe] magnesium ion exchange activity [moa] osmotic activity [moa] osmotic laxative [epc] phosphate binder [epc] phosphate chelating activity [moa] potassium compounds [cs] potassium salt [epc] stimulation large intestine fluid/electrolyte secretion [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 55792007
Hyphenated Format 55792-007

Supplemental Identifiers

UPC
0355792007103
UNII
5SL0G7R0OK M4I0D6VV5M DE08037SAB 660YQ98I10 8MDF5V39QO 451W47IQ8X SE337SVY37

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name elliotts b (source: ndc)
Generic Name sodium cation, sodium bicarbonate, anhydrous dextrose, magnesium sulfate, potassium chloride, calcium chloride, sodium phosphate (source: ndc)
Application Number NDA020577 (source: ndc)
Routes
INTRATHECAL
source: ndc

Resolved Composition

Strengths
  • 8 mg/10mL
  • 2 mg/10mL
  • 3 mg/10mL
  • 19 mg/10mL
  • 73 mg/10mL
source: ndc
Packaging
  • 10 AMPULE in 1 BOX (55792-007-10) / 10 mL in 1 AMPULE (55792-007-01)
source: ndc

Packages (1)

55792-007-10 10 AMPULE in 1 BOX (55792-007-10) / 10 mL in 1 AMPULE (55792-007-01)

Ingredients (7)

anhydrous dextrose (8 mg/10mL) calcium chloride (2 mg/10mL) magnesium sulfate, unspecified form (3 mg/10mL) potassium chloride (3 mg/10mL) sodium bicarbonate (19 mg/10mL) sodium chloride (73 mg/10mL) sodium phosphate (2 mg/10mL)

Linked Drug Pages (1)

Elliotts B ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRATHECAL"], "spl_id": "4a638cd1-6922-477a-aa17-a70865ae0bd8", "openfda": {"upc": ["0355792007103"], "unii": ["5SL0G7R0OK", "M4I0D6VV5M", "DE08037SAB", "660YQ98I10", "8MDF5V39QO", "451W47IQ8X", "SE337SVY37"], "spl_set_id": ["08036dbd-55b3-47b9-9890-000f253544f3"], "manufacturer_name": ["Lukare Medical, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 AMPULE in 1 BOX (55792-007-10)  / 10 mL in 1 AMPULE (55792-007-01)", "package_ndc": "55792-007-10", "marketing_start_date": "20130604"}], "brand_name": "Elliotts B", "product_id": "55792-007_4a638cd1-6922-477a-aa17-a70865ae0bd8", "dosage_form": "INJECTION", "pharm_class": ["Alkalinizing Activity [MoA]", "Blood Coagulation Factor [EPC]", "Calcium [CS]", "Calculi Dissolution Agent [EPC]", "Cations", "Divalent [CS]", "Increased Coagulation Factor Activity [PE]", "Increased Large Intestinal Motility [PE]", "Increased Large Intestinal Motility [PE]", "Increased Large Intestinal Motility [PE]", "Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]", "Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]", "Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]", "Inhibition Small Intestine Fluid/Electrolyte Absorption [PE]", "Magnesium Ion Exchange Activity [MoA]", "Osmotic Activity [MoA]", "Osmotic Activity [MoA]", "Osmotic Activity [MoA]", "Osmotic Laxative [EPC]", "Osmotic Laxative [EPC]", "Osmotic Laxative [EPC]", "Phosphate Binder [EPC]", "Phosphate Chelating Activity [MoA]", "Potassium Compounds [CS]", "Potassium Salt [EPC]", "Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]"], "product_ndc": "55792-007", "generic_name": "sodium cation, sodium bicarbonate, anhydrous dextrose, magnesium sulfate, potassium chloride, calcium chloride, sodium phosphate", "labeler_name": "Lukare Medical, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Elliotts B", "active_ingredients": [{"name": "ANHYDROUS DEXTROSE", "strength": "8 mg/10mL"}, {"name": "CALCIUM CHLORIDE", "strength": "2 mg/10mL"}, {"name": "MAGNESIUM SULFATE, UNSPECIFIED FORM", "strength": "3 mg/10mL"}, {"name": "POTASSIUM CHLORIDE", "strength": "3 mg/10mL"}, {"name": "SODIUM BICARBONATE", "strength": "19 mg/10mL"}, {"name": "SODIUM CHLORIDE", "strength": "73 mg/10mL"}, {"name": "SODIUM PHOSPHATE", "strength": "2 mg/10mL"}], "application_number": "NDA020577", "marketing_category": "NDA", "marketing_start_date": "20130604", "listing_expiration_date": "20261231"}