Package 49609-102-01

Brand: sodium fluoride f 18

Generic: sodium fluoride f-18
NDC Package

Package Facts

Identity

Package NDC 49609-102-01
Digits Only 4960910201
Product NDC 49609-102
Description

30 mL in 1 VIAL, MULTI-DOSE (49609-102-01)

Marketing

Marketing Status
Marketed Since 2011-12-08
Brand sodium fluoride f 18
Generic sodium fluoride f-18
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "31e5cd99-015b-86fa-e063-6394a90ad41b", "openfda": {"unii": ["9L75099X6R"], "spl_set_id": ["2bbd8f48-fdf9-45cb-8305-124a03f7a52c"], "manufacturer_name": ["SOFIE Co."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 mL in 1 VIAL, MULTI-DOSE (49609-102-01)", "package_ndc": "49609-102-01", "marketing_start_date": "20111208"}], "brand_name": "Sodium Fluoride F 18", "product_id": "49609-102_31e5cd99-015b-86fa-e063-6394a90ad41b", "dosage_form": "INJECTION", "pharm_class": ["Radioactive Diagnostic Agent [EPC]", "Radiopharmaceutical Activity [MoA]"], "product_ndc": "49609-102", "generic_name": "SODIUM FLUORIDE F-18", "labeler_name": "SOFIE Co.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sodium Fluoride F 18", "active_ingredients": [{"name": "SODIUM FLUORIDE F-18", "strength": "200 mCi/mL"}], "application_number": "ANDA203592", "marketing_category": "ANDA", "marketing_start_date": "20111208", "listing_expiration_date": "20261231"}