suflave
Generic: polyethylene glycol 3350, sodium sulfate, potassium chloride, magnesium sulfate, and sodium chloride for oral solution
Labeler: braintree laboratories, inc.Drug Facts
Product Profile
Brand Name
suflave
Generic Name
polyethylene glycol 3350, sodium sulfate, potassium chloride, magnesium sulfate, and sodium chloride for oral solution
Labeler
braintree laboratories, inc.
Dosage Form
KIT
Manufacturer
Identifiers & Regulatory
Product NDC
52268-550
Product ID
52268-550_ff5c09e0-dd90-12a1-e053-6294a90ab8a9
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA
Application Number
NDA215344
Listing Expiration
2026-12-31
Marketing Start
2023-06-15
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
52268550
Hyphenated Format
52268-550
Supplemental Identifiers
RxCUI
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
suflave (source: ndc)
Generic Name
polyethylene glycol 3350, sodium sulfate, potassium chloride, magnesium sulfate, and sodium chloride for oral solution (source: ndc)
Application Number
NDA215344 (source: ndc)
Resolved Composition
Strengths
- 178.7 g
- 7.3 g
- 1.12 g
- 0.9 g
- 0.5 g
Packaging
- 1 KIT in 1 KIT (52268-550-01)
Packages (1)
Ingredients (0)
No ingredient records.
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"spl_id": "ff5c09e0-dd90-12a1-e053-6294a90ab8a9", "openfda": {"rxcui": ["2641142", "2641143", "2641144"], "spl_set_id": ["546cfc44-791c-4524-99a9-6a0af96c4ec8"], "manufacturer_name": ["Braintree Laboratories, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 KIT in 1 KIT (52268-550-01)", "package_ndc": "52268-550-01", "marketing_start_date": "20230615"}], "brand_name": "SUFLAVE", "product_id": "52268-550_ff5c09e0-dd90-12a1-e053-6294a90ab8a9", "dosage_form": "KIT", "product_ndc": "52268-550", "generic_name": "polyethylene glycol 3350, sodium sulfate, potassium chloride, magnesium sulfate, and sodium chloride for oral solution", "labeler_name": "Braintree Laboratories, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "SUFLAVE", "application_number": "NDA215344", "marketing_category": "NDA", "marketing_start_date": "20230615", "listing_expiration_date": "20261231"}