Coral Drugs Private Limited
NDC Database

Coral Drugs Private Limited

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 2025-10-18
  • Data Source FDA
  • First Marketing Date 2016-02-25
Company Overview

Company

Coral Drugs Private Limited

Country

India

Website

Visit Website

Email

contact@coraldrugs.com

Social Profiles

LinkedIn
Company Snapshot

Coral Drugs Private Limited

1001, Akash Deep Building 26-A, Barakhamba Road New Delhi – 110001

India

coraldrugs.com/ contact@coraldrugs.com View on Map
NDC Records ( 13 records )
2020
13 Mar
Bulk Ingredient NDC: 49076-5201

Nonproprietary Name

Danazol

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Coral Drugs Private Limited

Marketing Category

BULK INGREDIENT

49076-5201

Substance

DANAZOL

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2020-03-13

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2020
01 Jun
Bulk Ingredient NDC: 49076-5251

Nonproprietary Name

Danazol

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Coral Drugs Private Limited

Marketing Category

BULK INGREDIENT

49076-5251

Substance

DANAZOL

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2020-06-01

End Marketing Date

-

Listing Record Certified Through

2027-12-31

2018
26 Oct
Bulk Ingredient NDC: 49076-5501

Nonproprietary Name

Fluticasone Propionate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Coral Drugs Private Limited

Marketing Category

BULK INGREDIENT

49076-5501

Substance

FLUTICASONE PROPIONATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2018-10-26

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2025
08 Aug
Bulk Ingredient NDC: 49076-5603

Nonproprietary Name

Mometasone Furoate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Coral Drugs Private Limited

Marketing Category

BULK INGREDIENT

49076-5603

Substance

MOMETASONE FUROATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2025-08-08

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2025
18 Oct
Bulk Ingredient NDC: 49076-5701

Nonproprietary Name

Mometasone Furoate Monohydrate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Coral Drugs Private Limited

Marketing Category

BULK INGREDIENT

49076-5701

Substance

MOMETASONE FUROATE MONOHYDRATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2025-10-18

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2025
17 Oct
Bulk Ingredient NDC: 49076-5702

Nonproprietary Name

Mometasone Furoate Monohydrate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Coral Drugs Private Limited

Marketing Category

BULK INGREDIENT

49076-5702

Substance

MOMETASONE FUROATE MONOHYDRATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2025-10-17

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2017
02 Nov
Bulk Ingredient NDC: 49076-6111

Nonproprietary Name

Budesonide

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Coral Drugs Private Limited

Marketing Category

BULK INGREDIENT

49076-6111

Substance

BUDESONIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2017-11-02

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2022
25 Feb
Bulk Ingredient NDC: 49076-6451

Nonproprietary Name

Fluticasone Furoate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Coral Drugs Private Limited

Marketing Category

BULK INGREDIENT

49076-6451

Substance

FLUTICASONE FUROATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2022-02-25

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2022
02 Mar
Bulk Ingredient NDC: 49076-6452

Nonproprietary Name

Fluticasone Furoate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Coral Drugs Private Limited

Marketing Category

BULK INGREDIENT

49076-6452

Substance

FLUTICASONE FUROATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2022-03-02

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2018
09 Apr
Bulk Ingredient NDC: 49076-6701

Nonproprietary Name

Triamcinolone Acetonide

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Coral Drugs Private Limited

Marketing Category

BULK INGREDIENT

49076-6701

Substance

.DELTA.14-TRIAMCINOLONE ACETONIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2018-04-09

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2016
25 Feb
Bulk Ingredient NDC: 49076-7001

Nonproprietary Name

Formoterol Fumarate Dihydrate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Coral Drugs Private Limited

Marketing Category

BULK INGREDIENT

49076-7001

Substance

FORMOTEROL FUMARATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2016-02-25

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2020
15 Jul
Bulk Ingredient NDC: 49076-7301

Nonproprietary Name

Isoflupredone Acetate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Coral Drugs Private Limited

Marketing Category

BULK INGREDIENT

49076-7301

Substance

ISOFLUPREDONE ACETATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2020-07-15

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2019
17 Jun
Bulk Ingredient NDC: 49076-7601

Nonproprietary Name

Azelastine Hydrochloride

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Coral Drugs Private Limited

Marketing Category

BULK INGREDIENT

49076-7601

Substance

AZELASTINE HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2019-06-17

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

49076-5201

Nonproprietary Name

Danazol

Labeler

Coral Drugs Private 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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