Package 63323-710-59

Brand: leucovorin calcium

Generic: leucovorin calcium
NDC Package

Package Facts

Identity

Package NDC 63323-710-59
Digits Only 6332371059
Product NDC 63323-710
Product ID 63323-710_b70ccebd-b847-41ff-8c30-9779461465e0
Description

1 VIAL in 1 BOX (63323-710-59) / 20 mL in 1 VIAL

Marketing

Marketing Status
Marketed Since 2010-09-18
Brand leucovorin calcium
Generic leucovorin calcium
Sample Package No

Linked Drug Pages (1)

Leucovorin Calcium ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "b70ccebd-b847-41ff-8c30-9779461465e0", "openfda": {"unii": ["RPR1R4C0P4"], "rxcui": ["1803937"], "spl_set_id": ["ab691d4e-e0d1-4ba1-9c7a-1cdcfcc3c17c"], "manufacturer_name": ["Fresenius Kabi USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 BOX (63323-710-59)  / 20 mL in 1 VIAL", "package_ndc": "63323-710-59", "marketing_start_date": "20100918"}], "brand_name": "Leucovorin Calcium", "product_id": "63323-710_b70ccebd-b847-41ff-8c30-9779461465e0", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Folate Analog [EPC]", "Folic Acid [CS]"], "product_ndc": "63323-710", "generic_name": "LEUCOVORIN CALCIUM", "labeler_name": "Fresenius Kabi USA, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Leucovorin Calcium", "active_ingredients": [{"name": "LEUCOVORIN CALCIUM", "strength": "200 mg/20mL"}], "application_number": "ANDA040258", "marketing_category": "ANDA", "marketing_start_date": "20100918", "listing_expiration_date": "20261231"}