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01 2STRIDES PHARMA

02 1ABBOTT

03 4ABLE

04 2ABRAXIS PHARM

05 1AILEX PHARMS LLC

06 5ALEMBIC

07 2ALEMBIC PHARMS LTD

08 1AMNEAL

09 2APPCO

10 4AUROBINDO PHARMA LTD

11 2B BRAUN

12 2BAUSCH

13 1BAXTER HLTHCARE

14 1BAXTER HLTHCARE CORP

15 2CADILA

16 2CADILA PHARMS LTD

17 1CASPER PHARMA LLC

18 2CHARTWELL MOLECULES

19 2CHARTWELL RX

20 1CHEMO RESEARCH SL

21 4COSETTE

22 4ENCUBE

23 2ESJAY PHARMA

24 2FLAMINGO PHARMS

25 4FOSUN PHARMA

26 3FOUGERA PHARMS

27 4GALDERMA LABS LP

28 1GLAND

29 1GLENMARK PHARMS LTD

30 2HALSEY

31 1HIKMA

32 1HOSPIRA

33 1INFORLIFE

34 3INNOGENIX

35 1INTL MEDICATION

36 2IVAX SUB TEVA PHARMS

37 2LABS AF

38 1LABS JUVISE

39 1LNK

40 2LUPIN LTD

41 2MUTUAL PHARM

42 1NOVAST LABS

43 2ORTHO MCNEIL PHARM

44 1PADAGIS ISRAEL

45 6PFIZER

46 1PH HEALTH

47 1PLIVA

48 1RISING

49 2SAPTALIS PHARMS

50 2SAVAGE LABS

51 1SOLARIS PHARMA CORP

52 2SUPERPHARM

53 2TARO

54 1TEVA PHARMS

55 1TEVA PHARMS USA

56 2UNICHEM

57 7WATSON LABS

58 1WATSON LABS INC

59 1ZYDUS LIFESCIENCES

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PharmaCompass

01

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothSynergice, a Strides Pharma initiative, is a new gen B2B platform for diverse portofolio needs.

RLD : No

TE Code : AB

METRONIDAZOLE

Brand Name : METRONIDAZOLE

Dosage Form : TABLET;ORAL

Dosage Strength : 500MG

Approval Date : 1985-01-29

Application Number : 70039

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

Strides Pharma Science

02

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothSynergice, a Strides Pharma initiative, is a new gen B2B platform for diverse portofolio needs.

RLD : No

TE Code : AB

METRONIDAZOLE

Brand Name : METRONIDAZOLE

Dosage Form : TABLET;ORAL

Dosage Strength : 250MG

Approval Date : 1985-01-29

Application Number : 70040

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

Strides Pharma Science

03

CPhI Korea
Not Confirmed
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CPhI Korea
Not Confirmed

METRONIDAZOLE

Brand Name : METRONIDAZOLE

Dosage Form : TABLET;ORAL

Dosage Strength : 250MG

Approval Date : 1982-09-17

Application Number : 18599

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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04

CPhI Korea
Not Confirmed
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CPhI Korea
Not Confirmed

METRONIDAZOLE

Brand Name : METRONIDAZOLE

Dosage Form : TABLET;ORAL

Dosage Strength : 500MG

Approval Date : 1984-02-13

Application Number : 18599

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

blank

05

CPhI Korea
Not Confirmed
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CPhI Korea
Not Confirmed

METRONIDAZOLE

Brand Name : METRONIDAZOLE

Dosage Form : TABLET;ORAL

Dosage Strength : 250MG

Approval Date : 1982-01-01

Application Number : 18517

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

blank

06

CPhI Korea
Not Confirmed
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CPhI Korea
Not Confirmed

METRONIDAZOLE

Brand Name : METRONIDAZOLE

Dosage Form : TABLET;ORAL

Dosage Strength : 500MG

Approval Date : 1982-05-05

Application Number : 18517

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

blank

07

CPhI Korea
Not Confirmed
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CPhI Korea
Not Confirmed

METRONIDAZOLE

Brand Name : FLAGYL

Dosage Form : TABLET;ORAL

Dosage Strength : 250MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1982-01-01

Application Number : 12623

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

blank

08

CPhI Korea
Not Confirmed
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CPhI Korea
Not Confirmed

METRONIDAZOLE

Brand Name : FLAGYL

Dosage Form : TABLET;ORAL

Dosage Strength : 500MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1982-01-01

Application Number : 12623

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

blank

09

CPhI Korea
Not Confirmed
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CPhI Korea
Not Confirmed

METRONIDAZOLE HYDROCHLORIDE

Brand Name : FLAGYL I.V.

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 500MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1982-01-01

Application Number : 18353

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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10

CPhI Korea
Not Confirmed
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CPhI Korea
Not Confirmed

METRONIDAZOLE

Brand Name : FLAGYL I.V. RTU IN PLASTIC CONTAINER

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 500MG/100ML

Approval Date : 1982-01-01

Application Number : 18353

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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