leucovorin calcium

Generic: leucovorin calcium

Labeler: slate run pharmaceuticals, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name leucovorin calcium
Generic Name leucovorin calcium
Labeler slate run pharmaceuticals, llc
Dosage Form INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes
INTRAMUSCULAR INTRAVENOUS
Active Ingredients

leucovorin calcium 500 mg/1

Manufacturer
Slate Run Pharmaceuticals, LLC

Identifiers & Regulatory

Product NDC 70436-120
Product ID 70436-120_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
folate analog [epc] folic acid [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 70436120
Hyphenated Format 70436-120

Supplemental Identifiers

RxCUI
237788 1803930 1803932 1803937 2055036
UNII
RPR1R4C0P4

Packaging Origin

Original Packager
true

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
INTRAMUSCULAR INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
source: ndc
Packaging
  • 500 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL (70436-120-80)
source: ndc

Packages (1)

70436-120-80 500 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL (70436-120-80)

Ingredients (1)

leucovorin calcium (500 mg/1)

Linked Drug Pages (1)

Leucovorin Calcium ndc-match (0.9)

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": "500 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL (70436-120-80)", "package_ndc": "70436-120-80", "marketing_start_date": "20230710"}], "brand_name": "Leucovorin Calcium", "product_id": "70436-120_2a4aaed3-885e-bc10-e063-6294a90a61af", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Folate Analog [EPC]", "Folic Acid [CS]"], "product_ndc": "70436-120", "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": "500 mg/1"}], "application_number": "ANDA217021", "marketing_category": "ANDA", "marketing_start_date": "20230710", "listing_expiration_date": "20261231"}