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01 1STRIDES PHARMA INTL
02 4ABIC
03 6ABRAXIS PHARM
04 5ACCORD HLTHCARE
05 3ALEMBIC
06 1AMNEAL PHARMS
07 14ASSERTIO SPECLTY
08 1AZURITY
09 5BARR
10 4BRISTOL
11 1BRISTOL MYERS
12 1BRISTOL MYERS SQUIBB
13 3CAPLIN ONE LABS
14 1DAITO
15 1DURAMED PHARMS BARR
16 1ELITE LABS INC
17 1EUGIA PHARMA
18 4EUGIA PHARMA SPECLTS
19 1EXTROVIS
20 4FRESENIUS KABI USA
21 1HETERO LABS LTD VI
22 6HIKMA
23 12HOSPIRA
24 1LOTUS PHARM CO LTD
25 10MEDEXUS
26 1MYLAN
27 1NORBROOK
28 8NORDIC GRP
29 4PHARMACHEMIE BV
30 1PHARMACHEMIE USA
31 6PHARMACIA AND UPJOHN
32 6QUAD PHARMS
33 3SAGENT PHARMS INC
34 4SHORLA
35 1SUN PHARM
36 1ZYDUS PHARMS
37 3Blank
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01 69INJECTABLE;INJECTION
02 6Injectable; Injection
03 1SOLUTION;INTRAVENOUS
04 5SOLUTION;ORAL
05 32SOLUTION;SUBCUTANEOUS
06 18TABLET;ORAL
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01 69DISCN
02 50RX
03 12Blank
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01 4ABITREXATE
02 4FOLEX
03 2FOLEX PFS
04 4JYLAMVO
05 1METHOTREXATE
06 1METHOTREXATE LPF
07 6METHOTREXATE PRESERVATIVE FREE
08 41METHOTREXATE SODIUM
09 25METHOTREXATE SODIUM PRESERVATIVE FREE
10 4MEXATE
11 1MEXATE-AQ
12 1MEXATE-AQ PRESERVED
13 8OTREXUP
14 6OTREXUP PFS
15 10RASUVO
16 8REDITREX
17 4TREXALL
18 1XATMEP
01 64No
02 55Yes
03 12Blank
RLD : Yes
TE Code :
Brand Name : METHOTREXATE SODIUM
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 2.5MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1982-01-01
Application Number : 8085
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
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RLD : Yes
TE Code :
Brand Name : METHOTREXATE SODIUM
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 20MG BASE/VIAL
Approval Date : 1982-01-01
Application Number : 11719
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :

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RLD : Yes
TE Code :
Brand Name : METHOTREXATE SODIUM
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 50MG BASE/VIAL
Approval Date : 1982-01-01
Application Number : 11719
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :

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RLD : Yes
TE Code :
Brand Name : METHOTREXATE SODIUM
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 2.5MG BASE/ML
Approval Date : 1982-01-01
Application Number : 11719
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :

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RLD : Yes
TE Code :
Brand Name : METHOTREXATE SODIUM
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 25MG BASE/ML
Approval Date : 1982-01-01
Application Number : 11719
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :

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RLD : Yes
TE Code :
Brand Name : METHOTREXATE SODIUM
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 100MG BASE/VIAL
Approval Date : 1982-01-01
Application Number : 11719
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :

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RLD : Yes
TE Code :
Brand Name : METHOTREXATE LPF
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 25MG BASE/ML
Approval Date : 1982-03-31
Application Number : 11719
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :

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RLD : Yes
TE Code :
Brand Name : METHOTREXATE SODIUM PRESERVATIVE FREE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 1GM BASE/VIAL
Approval Date : 1988-04-07
Application Number : 11719
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :

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RLD : Yes
TE Code : AP
Brand Name : METHOTREXATE SODIUM
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 50MG BASE/2ML (EQ 25MG BASE/ML)
Approval Date : 2004-12-15
Application Number : 11719
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AP

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RLD : Yes
TE Code :
Brand Name : METHOTREXATE PRESERVATIVE FREE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 2.5GM BASE/100ML (EQ 25MG BASE/ML)
Approval Date : 2005-04-13
Application Number : 11719
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
