leucovorin calcium
Generic: leucovorin calcium
Labeler: slate run pharmaceuticals, llcDrug Facts
Product Profile
Brand Name
leucovorin calcium
Generic Name
leucovorin calcium
Labeler
slate run pharmaceuticals, llc
Dosage Form
INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes
Active Ingredients
leucovorin calcium 50 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
70436-116
Product ID
70436-116_2a4aaed3-885e-bc10-e063-6294a90a61af
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA217021
Listing Expiration
2026-12-31
Marketing Start
2023-07-10
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
70436116
Hyphenated Format
70436-116
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
ANDA217021 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 50 mg/1
Packaging
- 10 VIAL in 1 BOX (70436-116-82) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL (70436-116-80)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
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": "10 VIAL in 1 BOX (70436-116-82) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL (70436-116-80)", "package_ndc": "70436-116-82", "marketing_start_date": "20230710"}], "brand_name": "Leucovorin Calcium", "product_id": "70436-116_2a4aaed3-885e-bc10-e063-6294a90a61af", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Folate Analog [EPC]", "Folic Acid [CS]"], "product_ndc": "70436-116", "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": "50 mg/1"}], "application_number": "ANDA217021", "marketing_category": "ANDA", "marketing_start_date": "20230710", "listing_expiration_date": "20261231"}