Agno Pharma
NDC Database

Agno Pharma

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 15
  • Latest Marketing Date 2024-12-04
  • Data Source FDA
  • First Marketing Date 2018-06-06
Company Overview

Company

Agno Pharma

Country

U.S.A

Social Profiles

Company Snapshot

Agno Pharma

752 56th Street,1st Floor New York, New York 11220

U.S.A

www.agnopharma.com/ info@agnopharma.com View on Map
NDC Records ( 15 records )
2022
01 Dec
Bulk Ingredient NDC: 57821-001

Nonproprietary Name

Chlorothiazide

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Agno Pharma Jiangsu

Marketing Category

BULK INGREDIENT

57821-001

Substance

CHLOROTHIAZIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2022-12-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2018
06 Jun
Bulk Ingredient NDC: 57821-002

Nonproprietary Name

Carmustine

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Agno Pharma Jiangsu

Marketing Category

BULK INGREDIENT

57821-002

Substance

CARMUSTINE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2018-06-06

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2020
03 Apr
Bulk Ingredient NDC: 57821-003

Nonproprietary Name

ISOSULFAN BLUE

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Agno Pharma Jiangsu

Marketing Category

BULK INGREDIENT

57821-003

Substance

ISOSULFAN BLUE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2020-04-03

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2020
01 Nov
Bulk Ingredient NDC: 57821-004

Nonproprietary Name

Cyclophosphamide

Dosage Form

POWDER

Strength

1 mg/mg

Labeler

Agno Pharma Jiangsu

Marketing Category

BULK INGREDIENT

57821-004

Substance

CYCLOPHOSPHAMIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2020-11-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2020
24 Apr
Bulk Ingredient NDC: 57821-005

Nonproprietary Name

SODIUM TETRADECYL SULFATE

Dosage Form

PASTE

Strength

1 kg/kg

Labeler

Agno Pharma Jiangsu

Marketing Category

BULK INGREDIENT

57821-005

Substance

SODIUM TETRADECYL SULFATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2020-04-24

End Marketing Date

-

Listing Record Certified Through

2027-12-31

2020
03 Apr
Bulk Ingredient NDC: 57821-006

Nonproprietary Name

CANNABIDIOL

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Agno Pharma Jiangsu

Marketing Category

BULK INGREDIENT

57821-006

Substance

CANNABIDIOL

Product Type

BULK INGREDIENT

DEA Schedule

CV

Start Marketing Date

2020-04-03

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2020
01 Nov
Bulk Ingredient NDC: 57821-007

Nonproprietary Name

ARIPIPRAZOLE MONOHYDRATE

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Agno Pharma Jiangsu

Marketing Category

BULK INGREDIENT

57821-007

Substance

ARIPIPRAZOLE MONOHYDRATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2020-11-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2020
01 Nov
Bulk Ingredient NDC: 57821-008

Nonproprietary Name

OLIVETOL

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Agno Pharma Jiangsu

Marketing Category

BULK INGREDIENT

57821-008

Substance

OLIVETOL

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2020-11-01

End Marketing Date

-

Listing Record Certified Through

2027-12-31

2020
01 Nov
Bulk Ingredient NDC: 57821-009

Nonproprietary Name

(plus) (1S,4R)-p-Menthadienol

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Agno Pharma Jiangsu

Marketing Category

BULK INGREDIENT

57821-009

Substance

2,8-P-MENTHADIEN-1-OL, CIS-(+)-

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2020-11-01

End Marketing Date

-

Listing Record Certified Through

2027-12-31

2020
01 Dec
Bulk Ingredient NDC: 57821-010

Nonproprietary Name

TETRABENAZINE

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Agno Pharma Jiangsu

Marketing Category

BULK INGREDIENT

57821-010

Substance

TETRABENAZINE, (+)-

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2020-12-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2022
26 Aug
Bulk Ingredient NDC: 57821-011

Nonproprietary Name

POLIDOCANOL

Dosage Form

LIQUID

Strength

1 kg/kg

Labeler

Agno Pharma Jiangsu

Marketing Category

BULK INGREDIENT

57821-011

Substance

POLIDOCANOL

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2022-08-26

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2022
26 Aug
Bulk Ingredient NDC: 57821-012

Nonproprietary Name

INDOMETHACIN

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Agno Pharma Jiangsu

Marketing Category

BULK INGREDIENT

57821-012

Substance

INDOMETHACIN

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2022-08-26

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2022
01 Dec
Bulk Ingredient NDC: 57821-013

Nonproprietary Name

Mannitol

Dosage Form

POWDER

Strength

1 g/g

Labeler

Agno Pharma Jiangsu

Marketing Category

BULK INGREDIENT

57821-013

Substance

MANNITOL

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2022-12-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2023
01 Dec
Bulk Ingredient NDC: 57821-014

Nonproprietary Name

TETRABENAZINE

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Agno Pharma Jiangsu

Marketing Category

BULK INGREDIENT

57821-014

Substance

TETRABENAZINE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2023-12-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2024
04 Dec
Bulk Ingredient NDC: 57821-015

Nonproprietary Name

Sulindac

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Agno Pharma Jiangsu

Marketing Category

BULK INGREDIENT

57821-015

Substance

SULINDAC

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2024-12-04

End Marketing Date

-

Listing Record Certified Through

2027-12-31

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NDC Type Breakdown
15 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

57821-001

Nonproprietary Name

Chlorothiazide

Labeler

Agno Pharma Jiangsu

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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