leucovorin calcium
Generic: leucovorin calcium
Labeler: sagent pharmaceuticalsDrug Facts
Product Profile
Brand Name
leucovorin calcium
Generic Name
leucovorin calcium
Labeler
sagent pharmaceuticals
Dosage Form
INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes
Active Ingredients
leucovorin calcium 500 mg/50mL
Manufacturer
Identifiers & Regulatory
Product NDC
25021-828
Product ID
25021-828_4619074b-a86b-41a6-bd98-76d15166764c
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA209110
Listing Expiration
2026-12-31
Marketing Start
2018-04-15
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
25021828
Hyphenated Format
25021-828
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
leucovorin calcium (source: ndc)
Generic Name
leucovorin calcium (source: ndc)
Application Number
ANDA209110 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 500 mg/50mL
Packaging
- 1 VIAL in 1 CARTON (25021-828-50) / 50 mL in 1 VIAL
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "4619074b-a86b-41a6-bd98-76d15166764c", "openfda": {"unii": ["RPR1R4C0P4"], "rxcui": ["2055036"], "spl_set_id": ["c0cbcbf6-6fd2-4cf3-877a-bb0fe3df4e59"], "manufacturer_name": ["Sagent Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (25021-828-50) / 50 mL in 1 VIAL", "package_ndc": "25021-828-50", "marketing_start_date": "20180415"}], "brand_name": "Leucovorin Calcium", "product_id": "25021-828_4619074b-a86b-41a6-bd98-76d15166764c", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Folate Analog [EPC]", "Folic Acid [CS]"], "product_ndc": "25021-828", "generic_name": "leucovorin calcium", "labeler_name": "Sagent Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Leucovorin Calcium", "active_ingredients": [{"name": "LEUCOVORIN CALCIUM", "strength": "500 mg/50mL"}], "application_number": "ANDA209110", "marketing_category": "ANDA", "marketing_start_date": "20180415", "listing_expiration_date": "20261231"}