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01 1STRIDES PHARMA

02 4MANKIND PHARMA

03 3ACTAVIS LABS FL INC

04 1ACTAVIS MID ATLANTIC

05 3ALEMBIC

06 4ALMATICA

07 1ALVOGEN

08 2AMNEAL PHARMS

09 1ANNORA PHARMA

10 1APPCO

11 3ATHEM

12 2AUROBINDO PHARMA

13 4AUROBINDO PHARMA USA

14 1BIOCON PHARMA

15 2CASPER PHARMA LLC

16 2CHARTWELL MOLECULAR

17 1CHARTWELL RX

18 2ELKINS SINN

19 2IMPAX LABS INC

20 1INVENTIA

21 2IVAX SUB TEVA PHARMS

22 3NOVEL LABS INC

23 1NOVITIUM PHARMA

24 1OMSAV PHARMA

25 3PROCTER AND GAMBLE

26 1RANBAXY LABS LTD

27 3SANDOZ

28 3SUN PHARM INDUSTRIES

29 1SUNNY

30 11WATSON LABS

31 1WATSON LABS INC

32 1WHITEWORTH TOWN PLSN

33 2ZYDUS PHARMS

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PharmaCompass

01

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothDelivering quality and niche Active Pharmaceutical Ingredients across the global from our USFDA-approved facility.

RLD : No

TE Code : AB

NITROFURANTOIN, MACROCRYSTALLINE

Brand Name : NITROFURANTOIN

Dosage Form : CAPSULE;ORAL

Dosage Strength : 25MG

Approval Date : 2023-03-21

Application Number : 217272

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

Company Banner

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

NITROFURANTOIN

Brand Name : NITROFURANTOIN

Dosage Form : SUSPENSION;ORAL

Dosage Strength : 25MG/5ML

Approval Date : 2013-08-14

Application Number : 201355

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

Strides Pharma Science

03

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothDelivering quality and niche Active Pharmaceutical Ingredients across the global from our USFDA-approved facility.

RLD : No

TE Code : AB

NITROFURANTOIN, MACROCRYSTALLINE

Brand Name : NITROFURANTOIN

Dosage Form : CAPSULE;ORAL

Dosage Strength : 50MG

Approval Date : 2023-03-21

Application Number : 217272

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

Company Banner

04

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothDelivering quality and niche Active Pharmaceutical Ingredients across the global from our USFDA-approved facility.

RLD : No

TE Code : AB

NITROFURANTOIN, MACROCRYSTALLINE

Brand Name : NITROFURANTOIN

Dosage Form : CAPSULE;ORAL

Dosage Strength : 100MG

Approval Date : 2023-03-21

Application Number : 217272

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

Company Banner

05

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothDelivering quality and niche Active Pharmaceutical Ingredients across the global from our USFDA-approved facility.

RLD : No

TE Code : AB

NITROFURANTOIN; NITROFURANTOIN, MACROCRYSTALLINE

Brand Name : NITROFURANTOIN (MONOHYDRATE/MACROCRYSTALS)

Dosage Form : CAPSULE;ORAL

Dosage Strength : 75MG;25MG

Approval Date : 2023-07-11

Application Number : 217357

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

Company Banner

06

KY/TN Water Professionals
Not Confirmed
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KY/TN Water Professionals
Not Confirmed

NITROFURANTOIN

Brand Name : FURADANTIN

Dosage Form : SUSPENSION;ORAL

Dosage Strength : 25MG/5ML

Approval Date : 1982-01-01

Application Number : 9175

RX/OTC/DISCN : RX

RLD : Yes

TE Code : AB

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07

KY/TN Water Professionals
Not Confirmed
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KY/TN Water Professionals
Not Confirmed

NITROFURANTOIN

Brand Name : FURADANTIN

Dosage Form : SUSPENSION;ORAL

Dosage Strength : 50MG/5ML

Approval Date : 2023-06-09

Application Number : 9175

RX/OTC/DISCN : RX

RLD : Yes

TE Code :

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08

KY/TN Water Professionals
Not Confirmed
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KY/TN Water Professionals
Not Confirmed

NITROFURANTOIN

Brand Name : FURADANTIN

Dosage Form : TABLET;ORAL

Dosage Strength : 50MG

Approval Date : 1982-01-01

Application Number : 8693

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

blank

09

KY/TN Water Professionals
Not Confirmed
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KY/TN Water Professionals
Not Confirmed

NITROFURANTOIN

Brand Name : FURADANTIN

Dosage Form : TABLET;ORAL

Dosage Strength : 100MG

Approval Date : 1982-01-01

Application Number : 8693

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

blank

10

KY/TN Water Professionals
Not Confirmed
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KY/TN Water Professionals
Not Confirmed

NITROFURANTOIN SODIUM

Brand Name : IVADANTIN

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 180MG BASE/VIAL

Approval Date : 1982-01-01

Application Number : 12402

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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