Package 70069-221-06

Brand: isosulfan blue

Generic: isosulfan blue
NDC Package

Package Facts

Identity

Package NDC 70069-221-06
Digits Only 7006922106
Product NDC 70069-221
Description

6 VIAL in 1 CARTON (70069-221-06) / 5 mL in 1 VIAL (70069-221-01)

Marketing

Marketing Status
Marketed Since 2019-07-23
Brand isosulfan blue
Generic isosulfan blue
Sample Package No

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"}