Porton Pharma Solutions
NDC Database

Porton Pharma Solutions

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 10
  • Latest Marketing Date 2026-05-13
  • Data Source FDA
  • First Marketing Date 2012-02-27
Company Overview

Company

Porton Pharma Solutions

Country

China

Website

Visit Website

Email

li.li10@portonpharma.com

Social Profiles

LinkedIn
Company Snapshot

Porton Pharma Solutions

Fangzheng Avenue, Shuitu, Beibei District, Chongqing ongqing, 401121

China

www.portonpharma.com/ li.li10@portonpharma.com View on Map
NDC Records ( 10 records )
2012
27 Feb
Bulk Ingredient NDC: 75877-0002

Nonproprietary Name

Nicotine

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Porton Pharma Solutions Ltd

Marketing Category

BULK INGREDIENT

75877-0002

Substance

NICOTINE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2012-02-27

End Marketing Date

-

Listing Record Certified Through

2027-12-31

2013
01 Jun
Bulk Ingredient NDC: 75877-0003

Nonproprietary Name

Propofol

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Porton Pharma Solutions Ltd

Marketing Category

BULK INGREDIENT

75877-0003

Substance

PROPOFOL

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2013-06-01

End Marketing Date

-

Listing Record Certified Through

2027-12-31

2014
10 Jan
Bulk Ingredient NDC: 75877-0004

Nonproprietary Name

Tiopronin

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Porton Pharma Solutions Ltd

Marketing Category

BULK INGREDIENT

75877-0004

Substance

TIOPRONIN

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2014-01-10

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2017
28 Nov
Bulk Ingredient NDC: 75877-0005

Nonproprietary Name

Mefloquine HCl

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Porton Pharma Solutions Ltd

Marketing Category

BULK INGREDIENT

75877-0005

Substance

MEFLOQUINE HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2017-11-28

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2017
28 Nov
Bulk Ingredient NDC: 75877-0006

Nonproprietary Name

Mefloquine HCl Micronized

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Porton Pharma Solutions Ltd

Marketing Category

BULK INGREDIENT

75877-0006

Substance

MEFLOQUINE HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2017-11-28

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2019
26 Mar
Bulk Ingredient NDC: 75877-0007

Nonproprietary Name

Darunavir Ethanolate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Porton Pharma Solutions Ltd

Marketing Category

BULK INGREDIENT

75877-0007

Substance

DARUNAVIR ETHANOLATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2019-03-26

End Marketing Date

-

Listing Record Certified Through

2027-12-31

2023
27 May
Bulk Ingredient NDC: 75877-0008

Nonproprietary Name

Vibegron

Dosage Form

POWDER

Strength

1 g/g

Labeler

Porton Pharma Solutions Ltd

Marketing Category

BULK INGREDIENT

75877-0008

Substance

VIBEGRON

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2023-05-27

End Marketing Date

-

Listing Record Certified Through

2027-12-31

2023
27 May
Bulk Ingredient NDC: 75877-0008

Nonproprietary Name

VIBEGRON

Dosage Form

POWDER

Strength

1 g/g

Labeler

Porton Pharma Solutions Ltd

Marketing Category

BULK INGREDIENT

75877-0008

Substance

VIBEGRON

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2023-05-27

End Marketing Date

-

Listing Record Certified Through

2027-12-31

2026
01 May
Bulk Ingredient NDC: 75877-0009

Nonproprietary Name

Orforglipron hemicalcium hydrate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Porton Pharma Solutions Ltd

Marketing Category

BULK INGREDIENT

75877-0009

Substance

ORFORGLIPRON HEMICALCIUM HYDRATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2026-05-01

End Marketing Date

-

Listing Record Certified Through

2027-12-31

2026
13 May
Bulk Ingredient NDC: 75877-0010

Nonproprietary Name

Ribociclib Succinate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Porton Pharma Solutions Ltd

Marketing Category

BULK INGREDIENT

75877-0010

Substance

RIBOCICLIB SUCCINATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2026-05-13

End Marketing Date

-

Listing Record Certified Through

2027-12-31

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NDC Type Breakdown
10 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

75877-0002

Nonproprietary Name

Nicotine

Labeler

Porton Pharma Solutions Ltd

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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