suprep bowel prep

Generic: sodium sulfate, potassium sulfate, magnesium sulfate

Labeler: braintree laboratories, inc.
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name suprep bowel prep
Generic Name sodium sulfate, potassium sulfate, magnesium sulfate
Labeler braintree laboratories, inc.
Dosage Form SOLUTION, CONCENTRATE
Routes
ORAL
Active Ingredients

magnesium sulfate, unspecified form 1.2 g/133.1mL, potassium sulfate 2.35 g/133.1mL, sodium sulfate 13.13 g/133.1mL

Manufacturer
Braintree Laboratories, Inc.

Identifiers & Regulatory

Product NDC 52268-112
Product ID 52268-112_9e639746-efc2-429f-b6c3-4d20a5f1a928
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA022372
Listing Expiration 2027-12-31
Marketing Start 2010-08-05

Pharmacologic Class

Classes
calculi dissolution agent [epc] 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] 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 52268112
Hyphenated Format 52268-112

Supplemental Identifiers

RxCUI
1001689 1001690 1120068 2390767 2390768
UPC
0352268011015 0352268111012
UNII
DE08037SAB 0YPR65R21J 1K573LC5TV

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 suprep bowel prep (source: ndc)
Generic Name sodium sulfate, potassium sulfate, magnesium sulfate (source: ndc)
Application Number NDA022372 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1.2 g/133.1mL
  • 2.35 g/133.1mL
  • 13.13 g/133.1mL
source: ndc
Packaging
  • 2 BOTTLE, PLASTIC in 1 CARTON (52268-112-01) / 133.1 mL in 1 BOTTLE, PLASTIC
source: ndc

Packages (1)

Ingredients (3)

magnesium sulfate, unspecified form (1.2 g/133.1mL) potassium sulfate (2.35 g/133.1mL) sodium sulfate (13.13 g/133.1mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "9e639746-efc2-429f-b6c3-4d20a5f1a928", "openfda": {"upc": ["0352268011015", "0352268111012"], "unii": ["DE08037SAB", "0YPR65R21J", "1K573LC5TV"], "rxcui": ["1001689", "1001690", "1120068", "2390767", "2390768"], "spl_set_id": ["2f5f06de-ee98-44c0-be7e-9a998d1e5c16"], "manufacturer_name": ["Braintree Laboratories, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 BOTTLE, PLASTIC in 1 CARTON (52268-112-01)  / 133.1 mL in 1 BOTTLE, PLASTIC", "package_ndc": "52268-112-01", "marketing_start_date": "20210105"}], "brand_name": "SUPREP Bowel Prep", "product_id": "52268-112_9e639746-efc2-429f-b6c3-4d20a5f1a928", "dosage_form": "SOLUTION, CONCENTRATE", "pharm_class": ["Calculi Dissolution Agent [EPC]", "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]", "Potassium Compounds [CS]", "Potassium Salt [EPC]", "Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]"], "product_ndc": "52268-112", "generic_name": "sodium sulfate, potassium sulfate, magnesium sulfate", "labeler_name": "Braintree Laboratories, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "SUPREP Bowel Prep", "active_ingredients": [{"name": "MAGNESIUM SULFATE, UNSPECIFIED FORM", "strength": "1.2 g/133.1mL"}, {"name": "POTASSIUM SULFATE", "strength": "2.35 g/133.1mL"}, {"name": "SODIUM SULFATE", "strength": "13.13 g/133.1mL"}], "application_number": "NDA022372", "marketing_category": "NDA", "marketing_start_date": "20100805", "listing_expiration_date": "20271231"}