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Athena Tramadol Hydrochloride Athena Tramadol Hydrochloride

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Approved Drug Products containing Alpharma Brand of Tramadol Hydrochloride listed in the FDA Orange Book. Original Data : FDA Website

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01 ATHENA (1)

02 STRIDES PHARMA (3)

03 ACCORD HLTHCARE (1)

04 ACI (1)

05 ACTAVIS ELIZABETH (4)

06 ALKEM LABS LTD (1)

07 AMNEAL PHARMS (2)

08 ANCHEN PHARMS (3)

09 APOTEX (1)

10 ASTA (1)

11 AUROBINDO PHARMA (1)

12 AUROBINDO PHARMA LTD (4)

13 CHARTWELL RX (1)

14 CIPHER PHARMS INC (4)

15 CSPC OUYI PHARM CO (1)

16 GRAVITI PHARMS (2)

17 IPCA LABS LTD (1)

18 IVAX SUB TEVA PHARMS (1)

19 JANSSEN PHARMS (3)

20 KOWA PHARMS (1)

21 LUPIN LTD (3)

22 MACLEODS PHARMS LTD (2)

23 MERRO PHARM USA (1)

24 MICRO LABS LTD INDIA (1)

25 MYLAN (4)

26 MYLAN PHARMS INC (1)

27 NORTHSTAR HLTHCARE (1)

28 NOSTRUM LABS INC (1)

29 PLIVA (1)

30 PURDUE PHARMA (3)

31 RISING (1)

32 RUBICON (3)

33 SHIONOGI INC (1)

34 SPECGX LLC (1)

35 SUN PHARM (6)

36 SUN PHARM INDS INC (2)

37 SUN PHARM INDUSTRIES (1)

38 TEVA (1)

39 UNICHEM (1)

40 VALEANT PHARMS (3)

41 WATSON LABS (1)

42 ZYDUS PHARMS USA INC (2)

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01 CAPSULE, EXTENDED RELEASE;ORAL (4)

02 SOLUTION;ORAL (1)

03 TABLET, EXTENDED RELEASE;ORAL (30)

04 TABLET, ORALLY DISINTEGRATING;ORAL (1)

05 TABLET;ORAL (42)

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01 DISCN (44)

02 RX (34)

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01 CONZIP (4)

02 QDOLO (1)

03 RYBIX ODT (1)

04 RYZOLT (3)

05 SEGLENTIS (1)

06 TRAMADOL HYDROCHLORIDE (51)

07 TRAMADOL HYDROCHLORIDE AND ACETAMINOPHEN (11)

08 ULTRACET (1)

09 ULTRAM (2)

10 ULTRAM ER (3)

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01 No (63)

02 Yes (15)

TABLET, EXTENDED RELEASE;ORAL
100MG
2009-11-13
78783
TRAMADOL HYDROCHLORIDE
DISCN
No
TABLET, EXTENDED RELEASE;ORAL
200MG
2009-11-13
78783
TRAMADOL HYDROCHLORIDE
DISCN
No
TABLET, EXTENDED RELEASE;ORAL
300MG
2011-09-20
78783
TRAMADOL HYDROCHLORIDE
DISCN
No
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TABLET, EXTENDED RELEASE;ORAL
100MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
2005-09-08
21692
ULTRAM ER
DISCN
Yes
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TABLET, EXTENDED RELEASE;ORAL
200MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
2005-09-08
21692
ULTRAM ER
DISCN
Yes
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TABLET, EXTENDED RELEASE;ORAL
300MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
2005-09-08
21692
ULTRAM ER
DISCN
Yes
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TABLET;ORAL
100MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
1995-03-03
20281
ULTRAM
DISCN
Yes
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TABLET;ORAL
50MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
1995-03-03
20281
ULTRAM
DISCN
Yes
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TABLET;ORAL
325MG;37.5MG
2001-08-15
21123
ULTRACET
DISCN
Yes
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