J.B.Chemicals & Pharmaceuticals
NDC Database

J.B.Chemicals & Pharmaceuticals

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 9
  • Latest Marketing Date 2025-02-03
  • Data Source FDA
  • First Marketing Date 2009-09-28
Company Overview

Company

J.B.Chemicals & Pharmaceuticals

Country

India

Social Profiles

LinkedIn
Company Snapshot

J.B.Chemicals & Pharmaceuticals

Cnergy IT Park, 3rd floor Appa Saheb Marathe Marg, Prabhadevi, Mumbai 400025

India

jbcpl.com/ info@jbcpl.com View on Map
NDC Records ( 9 records )
2009
04 Nov
Bulk Ingredient NDC: 48589-0002

Nonproprietary Name

Diclofenac

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Unique Chemicals

Marketing Category

BULK INGREDIENT

48589-0002

Substance

DICLOFENAC

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2009-11-04

End Marketing Date

-

Listing Record Certified Through

2027-12-31

2009
28 Sep
Bulk Ingredient NDC: 48589-0003

Nonproprietary Name

Diclofenac Diethylamine

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Unique Chemicals

Marketing Category

BULK INGREDIENT

48589-0003

Substance

DICLOFENAC DIETHYLAMINE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2009-09-28

End Marketing Date

-

Listing Record Certified Through

2027-12-31

2009
04 Nov
Bulk Ingredient NDC: 48589-0004

Nonproprietary Name

Diclofenac Potassium

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Unique Chemicals

Marketing Category

BULK INGREDIENT

48589-0004

Substance

DICLOFENAC POTASSIUM

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2009-11-04

End Marketing Date

-

Listing Record Certified Through

2027-12-31

2009
04 Nov
Bulk Ingredient NDC: 48589-0005

Nonproprietary Name

Diclofenac Sodium

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Unique Chemicals

Marketing Category

BULK INGREDIENT

48589-0005

Substance

DICLOFENAC SODIUM

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2009-11-04

End Marketing Date

-

Listing Record Certified Through

2027-12-31

2009
23 Oct
Bulk Ingredient NDC: 48589-0006

Nonproprietary Name

Nifedipine

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Unique Chemicals

Marketing Category

BULK INGREDIENT

48589-0006

Substance

NIFEDIPINE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2009-10-23

End Marketing Date

-

Listing Record Certified Through

2027-12-31

2016
19 Sep
Bulk Ingredient NDC: 48589-0007

Nonproprietary Name

Atenolol

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Unique Chemicals

Marketing Category

BULK INGREDIENT

48589-0007

Substance

ATENOLOL

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2016-09-19

End Marketing Date

-

Listing Record Certified Through

2027-12-31

2021
01 Nov
Bulk Ingredient NDC: 48589-0008

Nonproprietary Name

Glipizide

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Unique Chemicals

Marketing Category

BULK INGREDIENT

48589-0008

Substance

GLIPIZIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2021-11-01

End Marketing Date

-

Listing Record Certified Through

2027-12-31

2024
12 Jul
Bulk Ingredient NDC: 48589-0009

Nonproprietary Name

Cilnidipine

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Unique Chemicals

Marketing Category

BULK INGREDIENT

48589-0009

Substance

CILNIDIPINE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2024-07-12

End Marketing Date

-

Listing Record Certified Through

2027-12-31

2025
03 Feb
Bulk Ingredient NDC: 48589-0010

Nonproprietary Name

Lithium Carbonate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Unique Chemicals

Marketing Category

BULK INGREDIENT

48589-0010

Substance

LITHIUM CARBONATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2025-02-03

End Marketing Date

-

Listing Record Certified Through

2026-12-31

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NDC Type Breakdown
9 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

48589-0002

Nonproprietary Name

Diclofenac

Labeler

Unique Chemicals

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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