Virupaksha Organics
NDC Database

Virupaksha Organics

NDC Database

National Drug Code (NDC) records including drug products, NDC numbers, nonproprietary names, dosage forms, strengths, labelers and marketing information.

Bulk Ingredient
  • Total Records 13
  • Latest Marketing Date 2025-12-27
  • Data Source FDA
  • First Marketing Date 2004-06-19
Company Overview

Company

Virupaksha Organics

Country

India

Website

Visit Website

Email

info@virupaksha.com

Social Profiles

LinkedIn X / Twitter
Company Snapshot

Virupaksha Organics

IDA Industrial Area, Hyderabad Telangana, 500037

India

virupaksha.com/ info@virupaksha.com View on Map
NDC Records ( 13 records )
2007
16 Oct
Bulk Ingredient NDC: 51686-0001

Nonproprietary Name

Fexofenadine Hydrochloride

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

VIRUPAKSHA ORGANICS LIMITED

Marketing Category

BULK INGREDIENT

51686-0001

Substance

FEXOFENADINE HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2007-10-16

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2010
16 Nov
Bulk Ingredient NDC: 51686-0002

Nonproprietary Name

CAPSAICIN

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

VIRUPAKSHA ORGANICS LIMITED

Marketing Category

BULK INGREDIENT

51686-0002

Substance

CAPSAICIN

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2010-11-16

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2010
16 Nov
Bulk Ingredient NDC: 51686-0003

Nonproprietary Name

CAPSAICIN

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

VIRUPAKSHA ORGANICS LIMITED

Marketing Category

BULK INGREDIENT

51686-0003

Substance

CAPSAICIN

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2010-11-16

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2007
16 Oct
Bulk Ingredient NDC: 51686-0004

Nonproprietary Name

Flurbiprofen

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

VIRUPAKSHA ORGANICS LIMITED

Marketing Category

BULK INGREDIENT

51686-0004

Substance

FLURBIPROFEN

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2007-10-16

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2022
11 Nov
Bulk Ingredient NDC: 51686-0005

Nonproprietary Name

Crisaborole

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Virupaksha Organics Limited

Marketing Category

BULK INGREDIENT

51686-0005

Substance

CRISABOROLE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2022-11-11

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2007
16 Oct
Bulk Ingredient NDC: 51686-0006

Nonproprietary Name

Fluconazole

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

VIRUPAKSHA ORGANICS LIMITED

Marketing Category

BULK INGREDIENT

51686-0006

Substance

FLUCONAZOLE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2007-10-16

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2024
03 Jan
Bulk Ingredient NDC: 51686-0007

Nonproprietary Name

Citalopram Hydrobromide

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Virupaksha Organics Limited

Marketing Category

BULK INGREDIENT

51686-0007

Substance

CITALOPRAM HYDROBROMIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2024-01-03

End Marketing Date

-

Listing Record Certified Through

2027-12-31

2004
19 Jun
Bulk Ingredient NDC: 51686-0009

Nonproprietary Name

Tramadol HCl

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Virupaksha Organics Limited

Marketing Category

BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING

51686-0009

Substance

TRAMADOL HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

CIV

Start Marketing Date

2004-06-19

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2022
13 Jan
Bulk Ingredient NDC: 51686-0011

Nonproprietary Name

Escitalopram Oxalate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Virupaksha Organics Limited

Marketing Category

BULK INGREDIENT

51686-0011

Substance

ESCITALOPRAM OXALATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2022-01-13

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2007
16 Oct
Bulk Ingredient NDC: 51686-0012

Nonproprietary Name

Efinaconazole

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

VIRUPAKSHA ORGANICS LIMITED

Marketing Category

BULK INGREDIENT

51686-0012

Substance

EFINACONAZOLE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2007-10-16

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2024
03 Dec
Bulk Ingredient NDC: 51686-0013

Nonproprietary Name

BILASTINE

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Virupaksha Organics Limited

Marketing Category

BULK INGREDIENT

51686-0013

Substance

BILASTINE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2024-12-03

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2024
03 Dec
Bulk Ingredient NDC: 51686-0014

Nonproprietary Name

Dextromethorphan Hydrobromide

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Virupaksha Organics Limited

Marketing Category

BULK INGREDIENT

51686-0014

Substance

DEXTROMETHORPHAN HYDRIODIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2024-12-03

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2025
27 Dec
Bulk Ingredient NDC: 51686-0015

Nonproprietary Name

Ranolazine

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Virupaksha Organics Limited

Marketing Category

BULK INGREDIENT

51686-0015

Substance

RANOLAZINE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2025-12-27

End Marketing Date

-

Listing Record Certified Through

2026-12-31

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NDC Type Breakdown
13 total
  • Bulk Ingredient
Official Source

NDC data is based on publicly available National Drug Code information from the U.S. Food and Drug Administration (FDA).

Visit FDA NDC Directory
NDC Record Details Preview

Explore important National Drug Code information available in the records above.

NDC

51686-0001

Nonproprietary Name

Fexofenadine Hydrochloride

Labeler

VIRUPAKSHA ORGANICS LIMITED

Dosage Form

POWDER

FDA NDC Data

National Drug Code information

Regular Updates

Data maintained from official sources

Structured Database

Searchable pharmaceutical data

Reliable Data

Organized NDC records

NDC data is based on publicly available U.S. Food and Drug Administration (FDA) National Drug Code information.

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