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
68001-418
Product ID
68001-418_d5ee26ca-d963-687f-e053-2a95a90a2a50
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA040335
Listing Expiration
2026-12-31
Marketing Start
2019-09-26
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
68001418
Hyphenated Format
68001-418
Supplemental Identifiers
RxCUI
UPC
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
ANDA040335 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 350 mg/17.5mL
Packaging
- 1 VIAL in 1 BOX, UNIT-DOSE (68001-418-38) / 17.5 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": "d5ee26ca-d963-687f-e053-2a95a90a2a50", "openfda": {"upc": ["0368001416368", "0368001417372", "0368001418386"], "unii": ["RPR1R4C0P4"], "rxcui": ["237788", "1803932", "1803937"], "spl_set_id": ["e9b47126-8b52-43ff-85c4-33d32b3d8326"], "manufacturer_name": ["BluePoint Laboratories"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 BOX, UNIT-DOSE (68001-418-38) / 17.5 mL in 1 VIAL", "package_ndc": "68001-418-38", "marketing_start_date": "20190926"}], "brand_name": "Leucovorin Calcium", "product_id": "68001-418_d5ee26ca-d963-687f-e053-2a95a90a2a50", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Folate Analog [EPC]", "Folic Acid [CS]"], "product_ndc": "68001-418", "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": "ANDA040335", "marketing_category": "ANDA", "marketing_start_date": "20190926", "listing_expiration_date": "20261231"}