Recordati
NDC Database

Recordati

NDC Database

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

Bulk Ingredient Drug for Further Processing
  • Total Records 16
  • Latest Marketing Date 2025-05-07
  • Data Source FDA
  • First Marketing Date 1969-01-01
All
16
View
Bulk Ingredient
2
View
Drug for Further Processing
14
View
Company Overview

Company

Recordati

Country

Italy

Social Profiles

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Company Snapshot

Recordati

Via Matteo Civitali, 1 20148 Milan

Italy

www.recordati.com/en/ svil@recordati.it View on Map
NDC Records ( 16 records )
2025
07 May
Bulk Ingredient NDC: 12711-0145

Nonproprietary Name

Osilodrostat phosphate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

RECORDATI INDUSTRIA CHIMICA E FARMACEUTICA SPA

Marketing Category

BULK INGREDIENT

12711-0145

Substance

OSILODROSTAT PHOSPHATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2025-05-07

End Marketing Date

-

Listing Record Certified Through

2027-12-31

2007
01 Feb
Drug for Further Processing NDC: 12711-4350

Nonproprietary Name

Diphenhydramine Citrate

Dosage Form

POWDER

Strength

25 kg/25kg

Labeler

RECORDATI INDUSTRIA CHIMICA E FARMACEUTICA SPA

Marketing Category

DRUG FOR FURTHER PROCESSING

12711-4350

Substance

DIPHENHYDRAMINE CITRATE

Product Type

DRUG FOR FURTHER PROCESSING

DEA Schedule

Start Marketing Date

2007-02-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

1980
01 Jul
Drug for Further Processing NDC: 12711-4367

Nonproprietary Name

Diphenhydramine Hydrochloride

Dosage Form

POWDER

Strength

25 kg/25kg

Labeler

RECORDATI INDUSTRIA CHIMICA E FARMACEUTICA SPA

Marketing Category

DRUG FOR FURTHER PROCESSING

12711-4367

Substance

DIPHENHYDRAMINE HYDROCHLORIDE

Product Type

DRUG FOR FURTHER PROCESSING

DEA Schedule

Start Marketing Date

1980-07-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2009
01 Oct
Drug for Further Processing NDC: 12711-4444

Nonproprietary Name

Phenytoin

Dosage Form

POWDER

Strength

50 kg/50kg

Labeler

RECORDATI INDUSTRIA CHIMICA E FARMACEUTICA SPA

Marketing Category

DRUG FOR FURTHER PROCESSING

12711-4444

Substance

PHENYTOIN

Product Type

DRUG FOR FURTHER PROCESSING

DEA Schedule

Start Marketing Date

2009-10-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

1982
01 Jul
Drug for Further Processing NDC: 12711-4445

Nonproprietary Name

Phenytoin Micronized

Dosage Form

POWDER

Strength

25 kg/25kg

Labeler

RECORDATI INDUSTRIA CHIMICA E FARMACEUTICA SPA

Marketing Category

DRUG FOR FURTHER PROCESSING

12711-4445

Substance

PHENYTOIN

Product Type

DRUG FOR FURTHER PROCESSING

DEA Schedule

Start Marketing Date

1982-07-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

1969
01 Jan
Drug for Further Processing NDC: 12711-4466

Nonproprietary Name

Phenytoin Sodium

Dosage Form

POWDER

Strength

25 kg/25kg

Labeler

RECORDATI INDUSTRIA CHIMICA E FARMACEUTICA SPA

Marketing Category

DRUG FOR FURTHER PROCESSING

12711-4466

Substance

PHENYTOIN SODIUM

Product Type

DRUG FOR FURTHER PROCESSING

DEA Schedule

Start Marketing Date

1969-01-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

1982
01 Jul
Drug for Further Processing NDC: 12711-4675

Nonproprietary Name

Dimenhydrinate

Dosage Form

POWDER

Strength

25 kg/25kg

Labeler

RECORDATI INDUSTRIA CHIMICA E FARMACEUTICA SPA

Marketing Category

DRUG FOR FURTHER PROCESSING

12711-4675

Substance

DIMENHYDRINATE

Product Type

DRUG FOR FURTHER PROCESSING

DEA Schedule

Start Marketing Date

1982-07-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

1992
01 Jan
Drug for Further Processing NDC: 12711-4820

Nonproprietary Name

Dobutamine Hydrochloride

Dosage Form

POWDER

Strength

25 kg/25kg

Labeler

RECORDATI INDUSTRIA CHIMICA E FARMACEUTICA SPA

Marketing Category

DRUG FOR FURTHER PROCESSING

12711-4820

Substance

DOBUTAMINE HYDROCHLORIDE

Product Type

DRUG FOR FURTHER PROCESSING

DEA Schedule

Start Marketing Date

1992-01-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2005
03 Jan
Drug for Further Processing NDC: 12711-5522

Nonproprietary Name

Flavoxate HCl

Dosage Form

POWDER

Strength

25 kg/25kg

Labeler

RECORDATI INDUSTRIA CHIMICA E FARMACEUTICA SPA

Marketing Category

DRUG FOR FURTHER PROCESSING

12711-5522

Substance

FLAVOXATE HYDROCHLORIDE

Product Type

DRUG FOR FURTHER PROCESSING

DEA Schedule

Start Marketing Date

2005-01-03

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2010
30 Jul
Drug for Further Processing NDC: 12711-5990

Nonproprietary Name

KETOROLAC TROMETHAMINE

Dosage Form

POWDER

Strength

25 kg/25kg

Labeler

RECORDATI INDUSTRIA CHIMICA E FARMACEUTICA SPA

Marketing Category

DRUG FOR FURTHER PROCESSING

12711-5990

Substance

KETOROLAC TROMETHAMINE

Product Type

DRUG FOR FURTHER PROCESSING

DEA Schedule

Start Marketing Date

2010-07-30

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2001
01 Jun
Drug for Further Processing NDC: 12711-7480

Nonproprietary Name

Papaverine HCl

Dosage Form

POWDER

Strength

25 kg/25kg

Labeler

RECORDATI INDUSTRIA CHIMICA E FARMACEUTICA SPA

Marketing Category

DRUG FOR FURTHER PROCESSING

12711-7480

Substance

PAPAVERINE HYDROCHLORIDE

Product Type

DRUG FOR FURTHER PROCESSING

DEA Schedule

Start Marketing Date

2001-06-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

1993
01 Jan
Drug for Further Processing NDC: 12711-7490

Nonproprietary Name

Pyridoxal-5-Phosphate

Dosage Form

POWDER

Strength

25 kg/25kg

Labeler

RECORDATI INDUSTRIA CHIMICA E FARMACEUTICA SPA

Marketing Category

DRUG FOR FURTHER PROCESSING

12711-7490

Substance

PYRIDOXAL PHOSPHATE ANHYDROUS

Product Type

DRUG FOR FURTHER PROCESSING

DEA Schedule

Start Marketing Date

1993-01-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

1983
01 Jan
Drug for Further Processing NDC: 12711-9279

Nonproprietary Name

Verapamil Hydrochloride

Dosage Form

POWDER

Strength

25 kg/25kg

Labeler

RECORDATI INDUSTRIA CHIMICA E FARMACEUTICA SPA

Marketing Category

DRUG FOR FURTHER PROCESSING

12711-9279

Substance

VERAPAMIL HYDROCHLORIDE

Product Type

DRUG FOR FURTHER PROCESSING

DEA Schedule

Start Marketing Date

1983-01-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2025
07 May
Bulk Ingredient NDC: 12711-9500

Nonproprietary Name

Osilodrostat phosphate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

RECORDATI INDUSTRIA CHIMICA E FARMACEUTICA SPA

Marketing Category

BULK INGREDIENT

12711-9500

Substance

OSILODROSTAT PHOSPHATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2025-05-07

End Marketing Date

-

Listing Record Certified Through

2027-12-31

2007
01 Jan
Drug for Further Processing NDC: 12711-9744

Nonproprietary Name

ACYCLOVIR

Dosage Form

POWDER

Strength

20 kg/20kg

Labeler

RECORDATI INDUSTRIA CHIMICA E FARMACEUTICA SPA

Marketing Category

DRUG FOR FURTHER PROCESSING

12711-9744

Substance

ACYCLOVIR

Product Type

DRUG FOR FURTHER PROCESSING

DEA Schedule

Start Marketing Date

2007-01-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

1993
01 Jan
Drug for Further Processing NDC: 12711-9755

Nonproprietary Name

Acyclovir

Dosage Form

POWDER

Strength

25 kg/25kg

Labeler

RECORDATI INDUSTRIA CHIMICA E FARMACEUTICA SPA

Marketing Category

DRUG FOR FURTHER PROCESSING

12711-9755

Substance

ACYCLOVIR

Product Type

DRUG FOR FURTHER PROCESSING

DEA Schedule

Start Marketing Date

1993-01-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

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NDC Type Breakdown
16 total
  • Bulk Ingredient
  • Drug for Further Processing
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

12711-0145

Nonproprietary Name

Osilodrostat phosphate

Labeler

RECORDATI INDUSTRIA CHIMICA E FARMACEUTICA SPA

Dosage Form

POWDER

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Data maintained from official sources

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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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