suprep bowel prep
Generic: sodium sulfate, potassium sulfate, magnesium sulfate
Labeler: braintree laboratories, inc.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
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
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
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
52268112
Hyphenated Format
52268-112
Supplemental Identifiers
RxCUI
UPC
UNII
Packaging Origin
Original Packager
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
source: ndc
Resolved Composition
Strengths
- 1.2 g/133.1mL
- 2.35 g/133.1mL
- 13.13 g/133.1mL
Packaging
- 2 BOTTLE, PLASTIC in 1 CARTON (52268-112-01) / 133.1 mL in 1 BOTTLE, PLASTIC
Packages (1)
Ingredients (3)
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"}