leucovorin calcium
Generic: leucovorin calcium
Labeler: glenmark pharmaceuticals inc., usaDrug Facts
Product Profile
Brand Name
leucovorin calcium
Generic Name
leucovorin calcium
Labeler
glenmark pharmaceuticals inc., usa
Dosage Form
INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes
Active Ingredients
leucovorin calcium 350 mg/17.5mL
Manufacturer
Identifiers & Regulatory
Product NDC
68462-767
Product ID
68462-767_79d023ab-7d77-48c1-8f47-ea322fd58c2b
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA218200
Listing Expiration
2026-12-31
Marketing Start
2025-11-12
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
68462767
Hyphenated Format
68462-767
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
ANDA218200 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 350 mg/17.5mL
Packaging
- 1 VIAL in 1 CARTON (68462-767-35) / 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": "79d023ab-7d77-48c1-8f47-ea322fd58c2b", "openfda": {"upc": ["0368462767351"], "unii": ["RPR1R4C0P4"], "rxcui": ["237788"], "spl_set_id": ["79d023ab-7d77-48c1-8f47-ea322fd58c2b"], "manufacturer_name": ["GLENMARK PHARMACEUTICALS INC., USA"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (68462-767-35) / 17.5 mL in 1 VIAL", "package_ndc": "68462-767-35", "marketing_start_date": "20251112"}], "brand_name": "Leucovorin Calcium", "product_id": "68462-767_79d023ab-7d77-48c1-8f47-ea322fd58c2b", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Folate Analog [EPC]", "Folic Acid [CS]"], "product_ndc": "68462-767", "generic_name": "Leucovorin Calcium", "labeler_name": "GLENMARK PHARMACEUTICALS INC., USA", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Leucovorin Calcium", "active_ingredients": [{"name": "LEUCOVORIN CALCIUM", "strength": "350 mg/17.5mL"}], "application_number": "ANDA218200", "marketing_category": "ANDA", "marketing_start_date": "20251112", "listing_expiration_date": "20261231"}