suflave

Generic: polyethylene glycol 3350, sodium sulfate, potassium chloride, magnesium sulfate, and sodium chloride for oral solution

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

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
Braintree Laboratories, Inc.

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
2641142 2641143 2641144

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 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
source: label
Packaging
  • 1 KIT in 1 KIT (52268-550-01)
source: ndc

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"}