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NDC 25021-0816-30 Leucovorin Calcium 350 mg/17.5mL Details
Leucovorin Calcium 350 mg/17.5mL
Leucovorin Calcium is a INTRAMUSCULAR; INTRAVENOUS INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Sagent Pharmaceuticals. The primary component is LEUCOVORIN CALCIUM.
MedlinePlus Drug Summary
Leucovorin is used to prevent harmful effects of methotrexate (Rheumatrex, Trexall; cancer chemotherapy medication) when methotrexate is used to treat certain types of cancer. Leucovorin is also used to treat people who have accidentally received an overdose of methotrexate or similar medications. Leucovorin is in a class of medications called folic acid analogs. It works by protecting healthy cells from the effects of methotrexate or similar medications while allowing methotrexate to enter and kill cancer cells.
Related Packages: 25021-0816-30Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Leucovorin
Product Information
| NDC | 25021-0816 |
|---|---|
| Product ID | 25021-816_ff2ba160-e2f9-4ab9-9e67-2409f02c923e |
| Associated GPIs | 21755040102160 |
| GCN Sequence Number | 044534 |
| GCN Sequence Number Description | leucovorin calcium VIAL 350 MG INJECTION |
| HIC3 | V1I |
| HIC3 Description | CHEMOTHERAPY RESCUE/ANTIDOTE AGENTS |
| GCN | 87553 |
| HICL Sequence Number | 001063 |
| HICL Sequence Number Description | LEUCOVORIN CALCIUM |
| Brand/Generic | Generic |
| Proprietary Name | Leucovorin Calcium |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | leucovorin calcium |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
| Route | INTRAMUSCULAR; INTRAVENOUS |
| Active Ingredient Strength | 350 |
| Active Ingredient Units | mg/17.5mL |
| Substance Name | LEUCOVORIN CALCIUM |
| Labeler Name | Sagent Pharmaceuticals |
| Pharmaceutical Class | Folate Analog [EPC], Folic Acid [CS] |
| DEA Schedule | n/a |
| Marketing Category | ANDA |
| Application Number | ANDA200855 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 25021-0816-30 (25021081630)
| NDC Package Code | 25021-816-30 |
|---|---|
| Billing NDC | 25021081630 |
| Package | 1 VIAL in 1 CARTON (25021-816-30) / 17.5 mL in 1 VIAL |
| Marketing Start Date | 2012-09-15 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |