Strides Pharma Science: Pioneering IP-driven formulations for niche finished dosage forms.
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01 1STRIDES PHARMA
02 4ABIC
03 6ABRAXIS PHARM
04 5ACCORD HLTHCARE
05 1ALEMBIC
06 1AMNEAL PHARMS
07 1AZURITY
08 5BARR
09 4BRISTOL
10 1BRISTOL MYERS
11 1BRISTOL MYERS SQUIBB
12 1DAITO
13 1DURAMED PHARMS BARR
14 1ELITE LABS INC
15 1EUGIA PHARMA
16 4EUGIA PHARMA SPECLTS
17 1EXTROVIS
18 4FRESENIUS KABI USA
19 6HIKMA
20 12HOSPIRA
21 1LOTUS PHARM CO LTD
22 10MEDEXUS
23 1MYLAN
24 1NORBROOK
25 8NORDIC GRP
26 14OTTER PHARMS
27 4PHARMACHEMIE BV
28 1PHARMACHEMIE USA
29 6PHARMACIA AND UPJOHN
30 6QUAD PHARMS
31 3SAGENT PHARMS INC
32 3SANDOZ
33 4SHORLA
34 1SUN PHARM
35 1ZYDUS PHARMS
36 3Blank
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01 66INJECTABLE;INJECTION
02 6Injectable; Injection
03 1SOLUTION;INTRAVENOUS
04 5SOLUTION;ORAL
05 32SOLUTION;SUBCUTANEOUS
06 18TABLET;ORAL
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01 62DISCN
02 54RX
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 38METHOTREXATE 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 61No
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Dosage Strength : EQ 2.5MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 :
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 :
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 :
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 :
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 :
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 :
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 :
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 :
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
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 :