Edmond Pharma
NDC Database

Edmond Pharma

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 7
  • Latest Marketing Date 2021-04-05
  • Data Source FDA
  • First Marketing Date 1998-05-01
Company Overview

Company

Edmond Pharma

Country

India

Website

Visit Website

Email

Info@edmondpharmaceuticals.com

Social Profiles

Company Snapshot

Edmond Pharma

7/r, 18th cross, sector-3, HSR Layout, Bangalore-560102

India

edmondpharmaceuticals.com/ Info@edmondpharmaceuticals.com View on Map
NDC Records ( 7 records )
2013
01 Jul
Bulk Ingredient NDC: 66583-0510

Nonproprietary Name

DEXMEDETOMIDINE HYDROCHLORIDE

Dosage Form

POWDER

Strength

1 g/g

Labeler

Edmond Pharma Srl

Marketing Category

BULK INGREDIENT

66583-0510

Substance

DEXMEDETOMIDINE HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2013-07-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2016
14 Jun
Bulk Ingredient NDC: 66583-0515

Nonproprietary Name

Clenbuterol HCl

Dosage Form

POWDER

Strength

1 g/g

Labeler

Edmond Pharma Srl

Marketing Category

BULK INGREDIENT

66583-0515

Substance

CLENBUTEROL HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2016-06-14

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2010
01 Oct
Bulk Ingredient NDC: 66583-0516

Nonproprietary Name

Lurasidone Hydrochloride

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Edmond Pharma Srl

Marketing Category

BULK INGREDIENT

66583-0516

Substance

LURASIDONE HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2010-10-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2016
14 Jun
Bulk Ingredient NDC: 66583-0520

Nonproprietary Name

Noradrenaline Bitartrate Monohydrate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Edmond Pharma Srl

Marketing Category

BULK INGREDIENT

66583-0520

Substance

NORADRENALINE HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2016-06-14

End Marketing Date

-

Listing Record Certified Through

2026-12-31

1998
01 May
Bulk Ingredient NDC: 66583-0610

Nonproprietary Name

Ropivacaine Hydrochloride Monohydrate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Edmond Pharma Srl

Marketing Category

BULK INGREDIENT

66583-0610

Substance

ROPIVACAINE HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

1998-05-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2021
01 Jan
Bulk Ingredient NDC: 66583-0710

Nonproprietary Name

LEVOBUPIVACAINE BASE

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Edmond Pharma Srl

Marketing Category

BULK INGREDIENT

66583-0710

Substance

LEVOBUPIVACAINE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2021-01-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2021
05 Apr
Bulk Ingredient NDC: 66583-0810

Nonproprietary Name

CHLOROPROCAINE HYDROCHLORIDE

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Edmond Pharma Srl

Marketing Category

BULK INGREDIENT

66583-0810

Substance

CHLOROPROCAINE HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2021-04-05

End Marketing Date

-

Listing Record Certified Through

2026-12-31

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NDC Type Breakdown
7 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).

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NDC Record Details Preview

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

NDC

66583-0510

Nonproprietary Name

DEXMEDETOMIDINE HYDROCHLORIDE

Labeler

Edmond Pharma Srl

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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