Package 0942-9601-12

Brand: intersol

Generic: platelet additive 3
NDC Package

Package Facts

Identity

Package NDC 0942-9601-12
Digits Only 0942960112
Product NDC 0942-9601
Description

500 mL in 1 BAG (0942-9601-12)

Marketing

Marketing Status
Marketed Since 2012-10-25
Brand intersol
Generic platelet additive 3
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "e525571e-fef3-485f-a9af-858c14a7ec55", "openfda": {"unii": ["4550K0SC9B", "451W47IQ8X", "GR686LBA74", "593YOG76RN", "B22547B95K"], "spl_set_id": ["e4f06c0b-7cb1-49c9-97a4-2cfc21298495"], "manufacturer_name": ["Fenwal, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 mL in 1 BAG (0942-9601-12)", "package_ndc": "0942-9601-12", "marketing_start_date": "20121025"}], "brand_name": "InterSol", "product_id": "0942-9601_e525571e-fef3-485f-a9af-858c14a7ec55", "dosage_form": "SOLUTION", "pharm_class": ["Acidifying Activity [MoA]", "Anti-coagulant [EPC]", "Calcium Chelating Activity [MoA]", "Calculi Dissolution Agent [EPC]", "Decreased Coagulation Factor Activity [PE]"], "product_ndc": "0942-9601", "generic_name": "Platelet Additive 3", "labeler_name": "Fenwal, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "InterSol", "active_ingredients": [{"name": "SODIUM ACETATE", "strength": "442 mg/100mL"}, {"name": "SODIUM CHLORIDE", "strength": "452 mg/100mL"}, {"name": "SODIUM PHOSPHATE, DIBASIC, UNSPECIFIED FORM", "strength": "305 mg/100mL"}, {"name": "SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE", "strength": "93 mg/100mL"}, {"name": "TRISODIUM CITRATE DIHYDRATE", "strength": "318 mg/100mL"}], "application_number": "BN080041", "marketing_category": "NDA", "marketing_start_date": "20121025", "listing_expiration_date": "20261231"}