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Approved Drug Products containing Nitropress listed in the FDA Orange Book. Original Data : FDA Website

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01 ABBVIE (1)

02 DR REDDYS (1)

03 SUN PHARM (1)

04 ABBOTT (1)

05 ABRAXIS PHARM (1)

06 AMNEAL (1)

07 AMPHASTAR PHARMS INC (1)

08 AVET LIFESCIENCES (1)

09 BAXTER HLTHCARE (1)

10 BE PHARMS (1)

11 CAPLIN (1)

12 CHARTWELL RX (1)

13 CIPLA (1)

14 EPIC PHARMA LLC (1)

15 EUGIA PHARMA (1)

16 EXELA PHARMA (3)

17 HAINAN POLY (3)

18 HAINAN POLY PHARM (1)

19 HOSPIRA (1)

20 MICRO LABS (1)

21 MYLAN (1)

22 MYLAN LABS LTD (1)

23 NEXUS (1)

24 ROCHE (1)

25 SAGENT PHARMS INC (1)

26 SOMERSET THERAPS LLC (1)

27 TEVA PARENTERAL (1)

28 VPNA (1)

29 XIROMED (1)

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01 INJECTABLE;INJECTION (27)

02 SOLUTION;INTRAVENOUS (6)

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01 DISCN (16)

02 RX (17)

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01 NIPRIDE (1)

02 NIPRIDE RTU IN SODIUM CHLORIDE 0.9% (3)

03 NITROPRESS (4)

04 SODIUM NITROPRUSSIDE (25)

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01 No (28)

02 Yes (5)

URL Supplier Web Content
INJECTABLE;INJECTION
50MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
1982-01-01
18450
NITROPRESS
DISCN
Yes
Abbvie Company Banner

EMWA 2024

Not Confirmed

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URL Supplier Web Content
INJECTABLE;INJECTION
25MG/ML
2019-04-10
210114
SODIUM NITROPRUSSIDE
RX
No
AP
URL Supplier Web Content
INJECTABLE;INJECTION
25MG/ML
2018-11-26
210467
SODIUM NITROPRUSSIDE
DISCN
No
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INJECTABLE;INJECTION
50MG/VIAL
1987-11-16
71555
NITROPRESS
DISCN
No
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INJECTABLE;INJECTION
50MG/VIAL
1985-01-17
70031
SODIUM NITROPRUSSIDE
DISCN
No
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INJECTABLE;INJECTION
25MG/ML
1988-08-01
71961
NITROPRESS
DISCN
No
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INJECTABLE;INJECTION
50MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
1982-07-28
18581
SODIUM NITROPRUSSIDE
DISCN
Yes
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INJECTABLE;INJECTION
50MG/VIAL
1982-01-01
17546
NIPRIDE
DISCN
No
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INJECTABLE;INJECTION
50MG/VIAL
1986-06-09
70566
NITROPRESS
DISCN
No
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INJECTABLE;INJECTION
25MG/ML
1992-03-30
73465
SODIUM NITROPRUSSIDE
DISCN
No
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