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01 1STRIDES PHARMA INTL
02 3ABIC
03 6ABRAXIS PHARM
04 5ACCORD HLTHCARE
05 2ALEMBIC
06 1AMNEAL PHARMS
07 13ASSERTIO SPECLTY
08 1AZURITY
09 5BARR
10 4BRISTOL
11 1BRISTOL MYERS
12 1BRISTOL MYERS SQUIBB
13 2CAPLIN 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 2HIKMA FARMACEUTICA
24 12HOSPIRA
25 1LOTUS PHARM CO LTD
26 6MEDEXUS
27 1MYLAN LABS LTD
28 1NORBROOK
29 8NORDIC GRP
30 4PHARMACHEMIE BV
31 1PHARMACHEMIE USA
32 5PHARMACIA AND UPJOHN
33 1PRINSTON INC
34 6QUAD PHARMS
35 2SAGENT PHARMS INC
36 2SHORLA
37 1SUN PHARM
38 1ZYDUS PHARMS
39 3Blank
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01 67INJECTABLE;INJECTION
02 6Injectable; Injection
03 1SOLUTION;INTRAVENOUS
04 3SOLUTION;ORAL
05 27SOLUTION;SUBCUTANEOUS
06 18TABLET;ORAL
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01 66DISCN
02 46RX
03 10Blank
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01 3ABITREXATE
02 1DOXORUBICIN HYDROCHLORIDE
03 4FOLEX
04 1FOLEX PFS
05 2JYLAMVO
06 1METHOTREXATE
07 1METHOTREXATE LPF
08 6METHOTREXATE PRESERVATIVE FREE
09 39METHOTREXATE SODIUM
10 23METHOTREXATE SODIUM PRESERVATIVE FREE
11 4MEXATE
12 1MEXATE-AQ
13 1MEXATE-AQ PRESERVED
14 2MILRINONE LACTATE IN PLASTIC CONTAINER
15 7OTREXUP
16 6OTREXUP PFS
17 6RASUVO
18 8REDITREX
19 4TREXALL
20 1VENLAFAXINE HYDROCHLORIDE
21 1XATMEP
01 62No
02 50Yes
03 10Blank
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Dosage Strength : EQ 2.5MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 :
