Package 65219-236-10

Brand: dextrose

Generic: dextrose monohydrate
NDC Package

Package Facts

Identity

Package NDC 65219-236-10
Digits Only 6521923610
Product NDC 65219-236
Product ID 65219-236_39549d47-5040-4b1f-8b46-f0dd95832e1e
Description

50 BAG in 1 CASE (65219-236-10) / 100 mL in 1 BAG (65219-236-01)

Marketing

Marketing Status
Marketed Since 2021-11-10
Brand dextrose
Generic dextrose monohydrate
Sample Package No

Linked Drug Pages (1)

Dextrose ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "39549d47-5040-4b1f-8b46-f0dd95832e1e", "openfda": {"unii": ["LX22YL083G"], "rxcui": ["1795607", "1795609", "1795610", "1795616"], "spl_set_id": ["bd250a46-d229-4e80-b5a1-b34169ccecc4"], "manufacturer_name": ["Fresenius Kabi USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "50 BAG in 1 CASE (65219-236-10)  / 100 mL in 1 BAG (65219-236-01)", "package_ndc": "65219-236-10", "marketing_start_date": "20211110"}], "brand_name": "Dextrose", "product_id": "65219-236_39549d47-5040-4b1f-8b46-f0dd95832e1e", "dosage_form": "INJECTION, SOLUTION", "product_ndc": "65219-236", "generic_name": "Dextrose Monohydrate", "labeler_name": "Fresenius Kabi USA, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dextrose", "active_ingredients": [{"name": "DEXTROSE MONOHYDRATE", "strength": "5000 mg/100mL"}], "application_number": "ANDA207449", "marketing_category": "ANDA", "marketing_start_date": "20161021", "listing_expiration_date": "20261231"}