Procos
NDC Database

Procos

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 14
  • Latest Marketing Date 2026-04-22
  • Data Source FDA
  • First Marketing Date 2010-12-10
Company Overview

Company

Procos

Country

Italy

Email

Social Profiles

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Company Snapshot

Procos

via G. Matteotti, 249, 28062 Cameri (Novara)

Italy

www.procos.it/ View on Map
NDC Records ( 14 records )
2010
28 Dec
Bulk Ingredient NDC: 46016-1042

Nonproprietary Name

TROSPIUM CHLORIDE

Dosage Form

POWDER

Strength

50 kg/50kg

Labeler

PROCOS SpA

Marketing Category

BULK INGREDIENT

46016-1042

Substance

TROSPIUM CHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2010-12-28

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2010
10 Dec
Bulk Ingredient NDC: 46016-1331

Nonproprietary Name

ILOPERIDONE MICRONIZED

Dosage Form

POWDER

Strength

50 kg/50kg

Labeler

PROCOS SpA

Marketing Category

BULK INGREDIENT

46016-1331

Substance

ILOPERIDONE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2010-12-10

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2011
01 Jul
Bulk Ingredient NDC: 46016-1332

Nonproprietary Name

ILOPERIDONE

Dosage Form

POWDER

Strength

50 kg/50kg

Labeler

PROCOS SpA

Marketing Category

BULK INGREDIENT

46016-1332

Substance

ILOPERIDONE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2011-07-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2025
24 Oct
Bulk Ingredient NDC: 46016-1360

Nonproprietary Name

Lotilaner

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

PROCOS SpA

Marketing Category

BULK INGREDIENT

46016-1360

Substance

LOTILANER

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2025-10-24

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2022
28 Nov
Bulk Ingredient NDC: 46016-1550

Nonproprietary Name

Istradefylline

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

PROCOS SpA

Marketing Category

BULK INGREDIENT

46016-1550

Substance

ISTRADEFYLLINE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2022-11-28

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2022
28 Nov
Bulk Ingredient NDC: 46016-1551

Nonproprietary Name

Istradefylline

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

PROCOS SpA

Marketing Category

BULK INGREDIENT

46016-1551

Substance

ISTRADEFYLLINE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2022-11-28

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2021
23 Apr
Bulk Ingredient NDC: 46016-1830

Nonproprietary Name

Tipiracil HCl

Dosage Form

POWDER

Strength

50 kg/50kg

Labeler

PROCOS SpA

Marketing Category

BULK INGREDIENT

46016-1830

Substance

TIPIRACIL HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2021-04-23

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2018
26 Nov
Bulk Ingredient NDC: 46016-2030

Nonproprietary Name

Clofazimine

Dosage Form

POWDER

Strength

50 kg/50kg

Labeler

PROCOS SpA

Marketing Category

BULK INGREDIENT

46016-2030

Substance

CLOFAZIMINE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2018-11-26

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2020
09 Apr
Bulk Ingredient NDC: 46016-2140

Nonproprietary Name

Lofexidine Hydrochloride

Dosage Form

POWDER

Strength

50 kg/50kg

Labeler

Procos SpA

Marketing Category

BULK INGREDIENT

46016-2140

Substance

LOFEXIDINE HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2020-04-09

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2023
04 Apr
Bulk Ingredient NDC: 46016-2220

Nonproprietary Name

N-METHYL AMISULPRIDE

Dosage Form

POWDER

Strength

50 kg/50kg

Labeler

Procos SpA

Marketing Category

BULK INGREDIENT

46016-2220

Substance

N-METHYL AMISULPRIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2023-04-04

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2020
08 Jul
Bulk Ingredient NDC: 46016-5450

Nonproprietary Name

AMINOLEVULINIC ACID

Dosage Form

POWDER

Strength

50 kg/50kg

Labeler

Procos SpA

Marketing Category

BULK INGREDIENT

46016-5450

Substance

AMINOLEVULINIC ACID

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2020-07-08

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2021
03 Nov
Bulk Ingredient NDC: 46016-7940

Nonproprietary Name

Methyl Aminolevulinate Hydrochloride

Dosage Form

POWDER

Strength

50 kg/50kg

Labeler

PROCOS SpA

Marketing Category

BULK INGREDIENT

46016-7940

Substance

METHYL AMINOLEVULINATE HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2021-11-03

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2026
22 Apr
Bulk Ingredient NDC: 46016-8390

Nonproprietary Name

gepirone hydrochloride

Dosage Form

POWDER

Strength

50 kg/50kg

Labeler

PROCOS SpA

Marketing Category

BULK INGREDIENT

46016-8390

Substance

GEPIRONE HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2026-04-22

End Marketing Date

-

Listing Record Certified Through

2027-12-31

2026
26 Feb
Bulk Ingredient NDC: 46016-9030

Nonproprietary Name

Pitolisant HCL

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

PROCOS SpA

Marketing Category

BULK INGREDIENT

46016-9030

Substance

PITOLISANT HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2026-02-26

End Marketing Date

-

Listing Record Certified Through

2027-12-31

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NDC Type Breakdown
14 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

46016-1042

Nonproprietary Name

TROSPIUM CHLORIDE

Labeler

PROCOS SpA

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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