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Approved Drug Products containing MolPort-001-685-316 listed in the FDA Orange Book. Original Data : FDA Website

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01 3TARO

02 1AUCTA

03 3BRECKENRIDGE PHARM

04 3ACTAVIS LABS FL INC

05 3AJANTA PHARMA LTD

06 1ALKEM LABS LTD

07 1AMNEAL PHARMS

08 3ANI PHARMS

09 3ANNORA PHARMA

10 3APOTEX

11 1BIOCON PHARMA

12 1BIONPHARMA

13 1CHARTWELL RX

14 3GLENMARK PHARMS LTD

15 1HETERO LABS LTD III

16 4HIKMA

17 3JUBILANT CADISTA

18 1MEDLEY PHARMS

19 4NOVARTIS

20 1RENEW PHARMS

21 7RUBICON

22 3SUN PHARM INDS

23 1SUN PHARM INDS LTD

24 3SUPERNUS PHARMS

25 3TWI PHARMS INC

26 3ZYDUS

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PharmaCompass

01

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothAucta is a global brand that creates better products from proven molecules.

RLD : No

TE Code : AB

OXCARBAZEPINE

Brand Name : OXCARBAZEPINE

Dosage Form : SUSPENSION;ORAL

Dosage Strength : 300MG/5ML

Approval Date : 2022-11-30

Application Number : 215332

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

Aucta Company Banner

02

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Not Confirmed

OXCARBAZEPINE

Brand Name : OXCARBAZEPINE

Dosage Form : TABLET;ORAL

Dosage Strength : 150MG

Approval Date : 2008-01-11

Application Number : 78069

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

Breckenridge Pharmaceutical

03

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Not Confirmed

OXCARBAZEPINE

Brand Name : OXCARBAZEPINE

Dosage Form : TABLET;ORAL

Dosage Strength : 150MG

Approval Date : 2007-11-15

Application Number : 77801

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

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04

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Not Confirmed

OXCARBAZEPINE

Brand Name : OXCARBAZEPINE

Dosage Form : TABLET;ORAL

Dosage Strength : 300MG

Approval Date : 2007-11-15

Application Number : 77801

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

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05

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Not Confirmed

OXCARBAZEPINE

Brand Name : OXCARBAZEPINE

Dosage Form : TABLET;ORAL

Dosage Strength : 600MG

Approval Date : 2007-11-15

Application Number : 77801

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

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06

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Not Confirmed

OXCARBAZEPINE

Brand Name : OXCARBAZEPINE

Dosage Form : TABLET;ORAL

Dosage Strength : 300MG

Approval Date : 2008-01-11

Application Number : 78069

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

Breckenridge Pharmaceutical

07

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Not Confirmed

OXCARBAZEPINE

Brand Name : OXCARBAZEPINE

Dosage Form : TABLET;ORAL

Dosage Strength : 600MG

Approval Date : 2008-01-11

Application Number : 78069

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

Breckenridge Pharmaceutical

08

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Not Confirmed
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Not Confirmed

OXCARBAZEPINE

Brand Name : TRILEPTAL

Dosage Form : TABLET;ORAL

Dosage Strength : 150MG

Approval Date : 2000-01-14

Application Number : 21014

RX/OTC/DISCN : RX

RLD : Yes

TE Code : AB

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09

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Not Confirmed
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Not Confirmed

OXCARBAZEPINE

Brand Name : TRILEPTAL

Dosage Form : TABLET;ORAL

Dosage Strength : 300MG

Approval Date : 2000-01-14

Application Number : 21014

RX/OTC/DISCN : RX

RLD : Yes

TE Code : AB

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10

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Not Confirmed
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Not Confirmed

OXCARBAZEPINE

Brand Name : TRILEPTAL

Dosage Form : TABLET;ORAL

Dosage Strength : 600MG

Approval Date : 2000-01-14

Application Number : 21014

RX/OTC/DISCN : RX

RLD : Yes

TE Code : AB

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