Package 0143-9558-01

Brand: levoleucovorin

Generic: levoleucovorin
NDC Package

Package Facts

Identity

Package NDC 0143-9558-01
Digits Only 0143955801
Product NDC 0143-9558
Description

1 VIAL in 1 BOX (0143-9558-01) / 5 mL in 1 VIAL

Marketing

Marketing Status
Marketed Since 2016-07-07
Brand levoleucovorin
Generic levoleucovorin
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "d5427bbc-8598-4e79-9aeb-b0a9317e3433", "openfda": {"unii": ["778XL6VBS8"], "rxcui": ["1720760"], "spl_set_id": ["54f01988-aac2-4b0e-9d20-b7f621a0cd50"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 BOX (0143-9558-01)  / 5 mL in 1 VIAL", "package_ndc": "0143-9558-01", "marketing_start_date": "20160707"}], "brand_name": "Levoleucovorin", "product_id": "0143-9558_d5427bbc-8598-4e79-9aeb-b0a9317e3433", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Folate Analog [EPC]", "Folic Acid [CS]"], "product_ndc": "0143-9558", "generic_name": "Levoleucovorin", "labeler_name": "Hikma Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Levoleucovorin", "active_ingredients": [{"name": "LEVOLEUCOVORIN CALCIUM", "strength": "50 mg/5mL"}], "application_number": "ANDA206263", "marketing_category": "ANDA", "marketing_start_date": "20160707", "listing_expiration_date": "20261231"}