01 2ABIC
02 1ABRAXIS PHARM
03 1AM REGENT
04 1ANI PHARMS
05 2BARR
06 2ELKINS SINN
07 4EPIC PHARMA LLC
08 4FRESENIUS KABI USA
09 7GLAXOSMITHKLINE
10 4HAINAN POLY
11 10HIKMA
12 7HOSPIRA
13 4LEADING
14 5MEITHEAL
15 3MYLAN LABS LTD
16 5NOVAST LABS
17 2PAR PHARM
18 3PHARMACHEMIE
19 2PHARMACHEMIE USA
20 4QUAD PHARMS
21 4SAGENT PHARMS
22 1SAGENT PHARMS INC
23 2TEVA PARENTERAL
24 2TEVA PHARMS USA
25 3XANODYNE PHARM
01 1FOR SOLUTION;ORAL
02 40INJECTABLE;INJECTION
03 4Injectable; Injection
04 12SOLUTION;INTRAMUSCULAR, INTRAVENOUS
05 28TABLET;ORAL
01 38DISCN
02 43RX
03 4Blank
01 60LEUCOVORIN CALCIUM
02 18LEUCOVORIN CALCIUM PRESERVATIVE FREE
03 7WELLCOVORIN
01 75No
02 6Yes
03 4Blank
RLD : Yes
TE Code :
Brand Name : WELLCOVORIN
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 5MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1983-07-08
Application Number : 18342
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Brand Name : WELLCOVORIN
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 25MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1983-07-08
Application Number : 18342
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : No
TE Code : AP
Brand Name : LEUCOVORIN CALCIUM PRESERVATIVE FREE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 200MG BASE/VIAL
Approval Date : 1995-05-23
Application Number : 40056
RX/OTC/DISCN : RX
RLD : No
TE Code : AP
RLD : Yes
TE Code :
Brand Name : LEUCOVORIN CALCIUM
Dosage Form : SOLUTION;INTRAMUSCULAR, INTRAVENOUS
Dosage Strength : EQ 3MG BASE/ML (EQ 3MG BASE/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1982-01-01
Application Number : 8107
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Brand Name : LEUCOVORIN CALCIUM
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 50MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1982-01-01
Application Number : 8107
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : No
TE Code :
Brand Name : LEUCOVORIN CALCIUM
Dosage Form : FOR SOLUTION;ORAL
Dosage Strength : EQ 60MG BASE/VIAL
Approval Date : 1987-01-30
Application Number : 8107
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : Yes
TE Code :
Brand Name : LEUCOVORIN CALCIUM
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 100MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1988-05-23
Application Number : 8107
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Brand Name : LEUCOVORIN CALCIUM
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 350MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1989-04-05
Application Number : 8107
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : No
TE Code :
Brand Name : LEUCOVORIN CALCIUM PRESERVATIVE FREE
Dosage Form : SOLUTION;INTRAMUSCULAR, INTRAVENOUS
Dosage Strength : EQ 100MG BASE/10ML (EQ 10MG BASE/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1997-06-25
Application Number : 40147
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Brand Name : LEUCOVORIN CALCIUM
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 5MG BASE
Approval Date : 1986-01-30
Application Number : 18459
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
LOOKING FOR A SUPPLIER?
