Package 70436-119-80

Brand: leucovorin calcium

Generic: leucovorin calcium
NDC Package

Package Facts

Identity

Package NDC 70436-119-80
Digits Only 7043611980
Product NDC 70436-119
Product ID 70436-119_2a4aaed3-885e-bc10-e063-6294a90a61af
Description

1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL (70436-119-80)

Marketing

Marketing Status
Marketed Since 2024-12-27
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": "2a4aaed3-885e-bc10-e063-6294a90a61af", "openfda": {"unii": ["RPR1R4C0P4"], "rxcui": ["237788", "1803930", "1803932", "1803937", "2055036"], "spl_set_id": ["d8bdd60c-9a1c-4ef4-ba6b-b911849128f1"], "manufacturer_name": ["Slate Run Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL (70436-119-80)", "package_ndc": "70436-119-80", "marketing_start_date": "20241227"}], "brand_name": "Leucovorin Calcium", "product_id": "70436-119_2a4aaed3-885e-bc10-e063-6294a90a61af", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Folate Analog [EPC]", "Folic Acid [CS]"], "product_ndc": "70436-119", "generic_name": "leucovorin calcium", "labeler_name": "Slate Run Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Leucovorin Calcium", "active_ingredients": [{"name": "LEUCOVORIN CALCIUM", "strength": "350 mg/1"}], "application_number": "ANDA217021", "marketing_category": "ANDA", "marketing_start_date": "20241227", "listing_expiration_date": "20261231"}