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01 2ABIC

02 1ABRAXIS PHARM

03 1AM REGENT

04 1ANI PHARMS

05 3AVYXA HOLDINGS

06 2BARR

07 2ELKINS SINN

08 4EPIC PHARMA LLC

09 4FRESENIUS KABI USA

10 1GLAND

11 7GLAXOSMITHKLINE

12 5HAINAN POLY

13 10HIKMA

14 7HOSPIRA

15 1INGENUS PHARMS LLC

16 4LEADING

17 5MEITHEAL

18 3MYLAN LABS LTD

19 4NOVAST LABS

20 2PAR PHARM

21 3PHARMACHEMIE

22 2PHARMACHEMIE USA

23 4QUAD PHARMS

24 4SAGENT PHARMS

25 1SAGENT PHARMS INC

26 2TEVA PARENTERAL

27 2TEVA PHARMS USA

28 3XANODYNE PHARM

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PharmaCompass

01

CGT Asia
Not Confirmed
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CGT Asia
Not Confirmed

LEUCOVORIN CALCIUM

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Dosage Strength : EQ 5MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 :

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02

CGT Asia
Not Confirmed
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CGT Asia
Not Confirmed

LEUCOVORIN CALCIUM

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Dosage Strength : EQ 25MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 :

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03

CGT Asia
Not Confirmed
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CGT Asia
Not Confirmed

LEUCOVORIN CALCIUM

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

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04

CGT Asia
Not Confirmed
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CGT Asia
Not Confirmed

LEUCOVORIN CALCIUM

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Dosage Strength : EQ 3MG BASE/ML (EQ 3MG BASE/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 :

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05

CGT Asia
Not Confirmed
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CGT Asia
Not Confirmed

LEUCOVORIN CALCIUM

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 :

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06

CGT Asia
Not Confirmed
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CGT Asia
Not Confirmed

LEUCOVORIN CALCIUM

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 :

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07

CGT Asia
Not Confirmed
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CGT Asia
Not Confirmed

LEUCOVORIN CALCIUM

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 :

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08

CGT Asia
Not Confirmed
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CGT Asia
Not Confirmed

LEUCOVORIN CALCIUM

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 :

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09

CGT Asia
Not Confirmed
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CGT Asia
Not Confirmed

LEUCOVORIN CALCIUM

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 :

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10

XANODYNE PHARM

Country
CGT Asia
Not Confirmed
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XANODYNE PHARM

Country
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CGT Asia
Not Confirmed

LEUCOVORIN CALCIUM

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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