Roquette
NDC Database

Roquette

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 6
  • Latest Marketing Date 2021-01-01
  • Data Source FDA
  • First Marketing Date 2014-05-07
Company Overview

Company

Roquette

Country

France

Website

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Company Snapshot

Roquette

1 rue de la Haute Loge, 62136 Lestrem

France

www.roquette.com/ View on Map
NDC Records ( 6 records )
2014
19 Jun
Bulk Ingredient NDC: 52647-001

Nonproprietary Name

DEXTROSE MONOHYDRATE

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Roquette America, Inc.

Marketing Category

BULK INGREDIENT

52647-001

Substance

DEXTROSE MONOHYDRATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2014-06-19

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2014
07 May
Bulk Ingredient NDC: 50516-001

Nonproprietary Name

DEXTROSE MONOHYDRATE

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Roquette Freres SA

Marketing Category

BULK INGREDIENT

50516-001

Substance

DEXTROSE MONOHYDRATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2014-05-07

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2014
07 May
Bulk Ingredient NDC: 50516-002

Nonproprietary Name

MANNITOL

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Roquette Freres SA

Marketing Category

BULK INGREDIENT

50516-002

Substance

MANNITOL

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2014-05-07

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2020
01 Aug
Bulk Ingredient NDC: 50516-003

Nonproprietary Name

ADRABETADEX

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Roquette Freres SA

Marketing Category

BULK INGREDIENT

50516-003

Substance

ADRABETADEX

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2020-08-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2020
01 Aug
Bulk Ingredient NDC: 50516-004

Nonproprietary Name

SODIUM GLUCONATE

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Roquette Freres SA

Marketing Category

BULK INGREDIENT

50516-004

Substance

SODIUM GLUCONATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2020-08-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2021
01 Jan
Bulk Ingredient NDC: 50516-005

Nonproprietary Name

SORBITOL

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Roquette Freres SA

Marketing Category

BULK INGREDIENT

50516-005

Substance

SORBITOL

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2021-01-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

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NDC Type Breakdown
6 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

52647-001

Nonproprietary Name

DEXTROSE MONOHYDRATE

Labeler

Roquette America, Inc.

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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