Trifarma
NDC Database

Trifarma

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 7
  • Latest Marketing Date 2013-05-12
  • Data Source FDA
  • First Marketing Date 2012-03-08
Company Overview

Company

Trifarma

Country

Italy

Social Profiles

Company Snapshot

Trifarma

Via G. Guarini Matteucci 1 20162 Milan,

Italy

www.trifarma.it/ trifarma@trifarma.it View on Map
NDC Records ( 7 records )
2012
20 Apr
Bulk Ingredient NDC: 46204-0002

Nonproprietary Name

Fluphenazine Hydrochloride

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Trifarma S.p.A

Marketing Category

BULK INGREDIENT

46204-0002

Substance

FLUPHENAZINE HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2012-04-20

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2013
12 May
Bulk Ingredient NDC: 46204-0003

Nonproprietary Name

Perphenazine

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Trifarma S.p.A

Marketing Category

BULK INGREDIENT

46204-0003

Substance

PERPHENAZINE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2013-05-12

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2012
03 May
Bulk Ingredient NDC: 46204-0006

Nonproprietary Name

Thioridazine Hydrochloride

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Trifarma S.p.A

Marketing Category

BULK INGREDIENT

46204-0006

Substance

THIORIDAZINE HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2012-05-03

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2012
04 May
Bulk Ingredient NDC: 46204-0007

Nonproprietary Name

Prochlorperazine

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Trifarma S.p.A

Marketing Category

BULK INGREDIENT

46204-0007

Substance

PROCHLORPERAZINE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2012-05-04

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2012
08 Mar
Bulk Ingredient NDC: 46204-0106

Nonproprietary Name

Prochlorperazine Maleate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Trifarma S.p.A

Marketing Category

BULK INGREDIENT

46204-0106

Substance

PROCHLORPERAZINE MALEATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2012-03-08

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2012
20 Mar
Bulk Ingredient NDC: 46204-0120

Nonproprietary Name

Clindamycin Phosphate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Trifarma S.p.A

Marketing Category

BULK INGREDIENT

46204-0120

Substance

CLINDAMYCIN PHOSPHATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2012-03-20

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2012
02 Aug
Bulk Ingredient NDC: 46204-0121

Nonproprietary Name

Prochlorperazine Edisylate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Trifarma S.p.A

Marketing Category

BULK INGREDIENT

46204-0121

Substance

PROCHLORPERAZINE EDISYLATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2012-08-02

End Marketing Date

-

Listing Record Certified Through

2026-12-31

Related Databases
  • FDA Inspections
    0 View
  • EDQM CEP
    0 View
  • KDMF
    0 View
  • Japan DMF
    0 View
  • Eudra GMP
    0 View
  • NDC Database
    7 View
  • FDA Approved Drugs Database
    0 View
  • Drug Prices in Switzerland
    0 View
NDC Type Breakdown
7 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

46204-0002

Nonproprietary Name

Fluphenazine Hydrochloride

Labeler

Trifarma S.p.A

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.

Create a New Buying Request

Fields marked with * are mandatory.

Please enter quantity.
Please select a unit.
Please select quality standard.
Please select request type.
Please provide product specifications.
Please enter additional details.
Please select shipping preference.
Notice: By submitting this buying request, the provided product details and requirements may be published publicly on our marketplace.