Package 81284-315-05

Brand: bludigo

Generic: indigotindisulfonate sodium
NDC Package

Package Facts

Identity

Package NDC 81284-315-05
Digits Only 8128431505
Product NDC 81284-315
Description

5 AMPULE in 1 CARTON (81284-315-05) / 5 mL in 1 AMPULE (81284-315-00)

Marketing

Marketing Status
Marketed Since 2022-09-06
Brand bludigo
Generic indigotindisulfonate sodium
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "2d60b6a4-17d2-4864-b01c-9862283da8de", "openfda": {"upc": ["0381284315050"], "unii": ["D3741U8K7L"], "spl_set_id": ["73f246c4-b127-452e-856f-134b56cb8870"], "manufacturer_name": ["Provepharm Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "5 AMPULE in 1 CARTON (81284-315-05)  / 5 mL in 1 AMPULE (81284-315-00)", "package_ndc": "81284-315-05", "marketing_start_date": "20220906"}], "brand_name": "BLUDIGO", "product_id": "81284-315_2d60b6a4-17d2-4864-b01c-9862283da8de", "dosage_form": "INJECTION", "pharm_class": ["Diagnostic Dye [EPC]", "Dyes [MoA]"], "product_ndc": "81284-315", "generic_name": "indigotindisulfonate sodium", "labeler_name": "Provepharm Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "BLUDIGO", "active_ingredients": [{"name": "INDIGOTINDISULFONATE SODIUM", "strength": "8 mg/mL"}], "application_number": "NDA216264", "marketing_category": "NDA", "marketing_start_date": "20220906", "listing_expiration_date": "20261231"}