leucovorin calcium
Generic: leucovorin calcium
Labeler: bluepoint laboratoriesDrug Facts
Product Profile
Brand Name
leucovorin calcium
Generic Name
leucovorin calcium
Labeler
bluepoint laboratories
Dosage Form
INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes
Active Ingredients
leucovorin calcium 350 mg/17.5mL
Manufacturer
Identifiers & Regulatory
Product NDC
68001-650
Product ID
68001-650_3ff11eb8-de81-1e0d-e063-6394a90a0f7c
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA216590
Listing Expiration
2026-12-31
Marketing Start
2025-05-10
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
68001650
Hyphenated Format
68001-650
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
ANDA216590 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 350 mg/17.5mL
Packaging
- 1 VIAL, SINGLE-DOSE in 1 CARTON (68001-650-38) / 17.5 mL in 1 VIAL, SINGLE-DOSE
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "3ff11eb8-de81-1e0d-e063-6394a90a0f7c", "openfda": {"unii": ["RPR1R4C0P4"], "rxcui": ["237788", "1803932", "1803937"], "spl_set_id": ["f579879c-7d53-4663-8ad8-84b8b645cda5"], "manufacturer_name": ["BluePoint Laboratories"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 CARTON (68001-650-38) / 17.5 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "68001-650-38", "marketing_start_date": "20250815"}], "brand_name": "leucovorin calcium", "product_id": "68001-650_3ff11eb8-de81-1e0d-e063-6394a90a0f7c", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Folate Analog [EPC]", "Folic Acid [CS]"], "product_ndc": "68001-650", "generic_name": "leucovorin calcium", "labeler_name": "BluePoint Laboratories", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "leucovorin calcium", "active_ingredients": [{"name": "LEUCOVORIN CALCIUM", "strength": "350 mg/17.5mL"}], "application_number": "ANDA216590", "marketing_category": "ANDA", "marketing_start_date": "20250510", "listing_expiration_date": "20261231"}