isosulfan blue

Generic: isosulfan blue

Labeler: somerset therapeutics, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name isosulfan blue
Generic Name isosulfan blue
Labeler somerset therapeutics, llc
Dosage Form INJECTION, SOLUTION
Routes
SUBCUTANEOUS
Active Ingredients

isosulfan blue 10 mg/mL

Manufacturer
Somerset Therapeutics, LLC

Identifiers & Regulatory

Product NDC 70069-221
Product ID 70069-221_ed436868-8729-4a79-b5b5-15c1b12bde81
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA210558
Listing Expiration 2026-12-31
Marketing Start 2019-07-23

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 70069221
Hyphenated Format 70069-221

Supplemental Identifiers

UNII
39N9K8S2A4

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 isosulfan blue (source: ndc)
Generic Name isosulfan blue (source: ndc)
Application Number ANDA210558 (source: ndc)
Routes
SUBCUTANEOUS
source: ndc

Resolved Composition

Strengths
  • 10 mg/mL
source: ndc
Packaging
  • 6 VIAL in 1 CARTON (70069-221-06) / 5 mL in 1 VIAL (70069-221-01)
source: ndc

Packages (1)

Ingredients (1)

isosulfan blue (10 mg/mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["SUBCUTANEOUS"], "spl_id": "ed436868-8729-4a79-b5b5-15c1b12bde81", "openfda": {"unii": ["39N9K8S2A4"], "spl_set_id": ["a4c7400a-ff36-4a76-aa84-7f91e303f937"], "manufacturer_name": ["Somerset Therapeutics, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "6 VIAL in 1 CARTON (70069-221-06)  / 5 mL in 1 VIAL (70069-221-01)", "package_ndc": "70069-221-06", "marketing_start_date": "20190723"}], "brand_name": "Isosulfan Blue", "product_id": "70069-221_ed436868-8729-4a79-b5b5-15c1b12bde81", "dosage_form": "INJECTION, SOLUTION", "product_ndc": "70069-221", "generic_name": "Isosulfan Blue", "labeler_name": "Somerset Therapeutics, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Isosulfan Blue", "active_ingredients": [{"name": "ISOSULFAN BLUE", "strength": "10 mg/mL"}], "application_number": "ANDA210558", "marketing_category": "ANDA", "marketing_start_date": "20190723", "listing_expiration_date": "20261231"}