Derivados Quimicos SAU
NDC Database

Derivados Quimicos SAU

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 2025-10-23
  • Data Source FDA
  • First Marketing Date 2008-12-29
Company Overview

Company

Derivados Quimicos SAU

Country

Spain

Website

Visit Website

Email

derivados@infagroup.com

Social Profiles

Company Snapshot

Derivados Quimicos SAU

Camino Viejo de pliego, S/N. 30820 Alcantarilla, Murcia

Spain

infagroup.com/ derivados@infagroup.com View on Map
NDC Records ( 13 records )
2008
29 Dec
Bulk Ingredient NDC: 59349-0002

Nonproprietary Name

Niclosamide

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Derivados Quimicos SAU

Marketing Category

BULK INGREDIENT

59349-0002

Substance

NICLOSAMIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2008-12-29

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2008
29 Dec
Bulk Ingredient NDC: 59349-0003

Nonproprietary Name

Meloxicam

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Derivados Quimicos SAU

Marketing Category

BULK INGREDIENT

59349-0003

Substance

MELOXICAM

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2008-12-29

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2010
06 Apr
Bulk Ingredient NDC: 59349-0005

Nonproprietary Name

Betaxolol Hydrochloride

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Derivados Quimicos SAU

Marketing Category

BULK INGREDIENT

59349-0005

Substance

BETAXOLOL HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2010-04-06

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2008
29 Dec
Bulk Ingredient NDC: 59349-0007

Nonproprietary Name

Terbinafine Hydrochloride

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Derivados Quimicos SAU

Marketing Category

BULK INGREDIENT

59349-0007

Substance

TERBINAFINE HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2008-12-29

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2008
29 Dec
Bulk Ingredient NDC: 59349-0008

Nonproprietary Name

Terbinafine

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Derivados Quimicos SAU

Marketing Category

BULK INGREDIENT

59349-0008

Substance

TERBINAFINE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2008-12-29

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2008
29 Dec
Bulk Ingredient NDC: 59349-0012

Nonproprietary Name

Itraconazole

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Derivados Quimicos SAU

Marketing Category

BULK INGREDIENT

59349-0012

Substance

ITRACONAZOLE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2008-12-29

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2017
11 Dec
Bulk Ingredient NDC: 59349-0015

Nonproprietary Name

Lansoprazole

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Derivados Quimicos SAU

Marketing Category

BULK INGREDIENT

59349-0015

Substance

LANSOPRAZOLE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2017-12-11

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2017
11 Dec
Bulk Ingredient NDC: 59349-0017

Nonproprietary Name

Sevelamer Hydrochloride

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Derivados Quimicos SAU

Marketing Category

BULK INGREDIENT

59349-0017

Substance

SEVELAMER HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2017-12-11

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2017
11 Dec
Bulk Ingredient NDC: 59349-0024

Nonproprietary Name

Niclosamide ethanolamine salt

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Derivados Quimicos SAU

Marketing Category

BULK INGREDIENT

59349-0024

Substance

NICLOSAMIDE-OLAMINE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2017-12-11

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2017
11 Dec
Bulk Ingredient NDC: 59349-0025

Nonproprietary Name

Labetalol Hydrochloride

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Derivados Quimicos SAU

Marketing Category

BULK INGREDIENT

59349-0025

Substance

LABETALOL HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2017-12-11

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2017
16 Feb
Bulk Ingredient NDC: 59349-0026

Nonproprietary Name

Trichlormethiazide

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Derivados Quimicos SAU

Marketing Category

BULK INGREDIENT

59349-0026

Substance

TRICHLORMETHIAZIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2017-02-16

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2024
07 Jun
Bulk Ingredient NDC: 59349-0040

Nonproprietary Name

Terbinafine Base

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Derivados Quimicos SAU

Marketing Category

BULK INGREDIENT

59349-0040

Substance

TERBINAFINE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2024-06-07

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2025
23 Oct
Bulk Ingredient NDC: 59349-0042

Nonproprietary Name

Domperidone

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Derivados Quimicos SAU

Marketing Category

BULK INGREDIENT

59349-0042

Substance

DOMPERIDONE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2025-10-23

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

59349-0002

Nonproprietary Name

Niclosamide

Labeler

Derivados Quimicos SAU

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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