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 1GLAND
10 7GLAXOSMITHKLINE
11 5HAINAN POLY
12 10HIKMA
13 7HOSPIRA
14 4LEADING
15 5MEITHEAL
16 3MYLAN LABS LTD
17 5NOVAST LABS
18 2PAR PHARM
19 3PHARMACHEMIE
20 2PHARMACHEMIE USA
21 4QUAD PHARMS
22 4SAGENT PHARMS
23 1SAGENT PHARMS INC
24 2TEVA PARENTERAL
25 2TEVA PHARMS USA
26 3XANODYNE PHARM
01 1FOR SOLUTION;ORAL
02 42INJECTABLE;INJECTION
03 4Injectable; Injection
04 12SOLUTION;INTRAMUSCULAR, INTRAVENOUS
05 28TABLET;ORAL
01 38DISCN
02 45RX
03 4Blank
01 62LEUCOVORIN CALCIUM
02 18LEUCOVORIN CALCIUM PRESERVATIVE FREE
03 7WELLCOVORIN
01 77No
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Dosage Strength : EQ 5MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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Dosage Strength : EQ 25MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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Dosage Strength : EQ 3MG BASE/ML (EQ 3MG BASE/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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Dosage Strength : EQ 50MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 :
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