Kreative Organics
NDC Database

Kreative Organics

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 8
  • Latest Marketing Date 2025-06-01
  • Data Source FDA
  • First Marketing Date 2023-02-01
Company Overview

Company

Kreative Organics

Country

India

Social Profiles

Company Snapshot

Kreative Organics

Plot No.1306, Road No.#65, Jubilee Hills, Hyderabad 500 033, Telangana

India

www.kreativeorganics.com/ sales@kreativeorganics.com View on Map
NDC Records ( 8 records )
2023
01 Mar
Bulk Ingredient NDC: 83221-001

Nonproprietary Name

BISACODYL

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

KREATIVE ACTIVES PRIVATE LIMITED

Marketing Category

BULK INGREDIENT

83221-001

Substance

BISACODYL

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2023-03-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2024
30 Nov
Bulk Ingredient NDC: 83221-002

Nonproprietary Name

Salsalate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

KREATIVE ACTIVES PRIVATE LIMITED

Marketing Category

BULK INGREDIENT

83221-002

Substance

SALSALATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2024-11-30

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2023
01 Feb
Bulk Ingredient NDC: 83221-003

Nonproprietary Name

ETODOLAC

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

KREATIVE ACTIVES PRIVATE LIMITED

Marketing Category

BULK INGREDIENT

83221-003

Substance

ETODOLAC

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2023-02-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2023
01 Mar
Bulk Ingredient NDC: 83221-004

Nonproprietary Name

METHENAMINE HIPPURATE

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

KREATIVE ACTIVES PRIVATE LIMITED

Marketing Category

BULK INGREDIENT

83221-004

Substance

METHENAMINE HIPPURATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2023-03-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2023
17 Oct
Bulk Ingredient NDC: 83221-005

Nonproprietary Name

Sodium Picosulfate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

KREATIVE ACTIVES PRIVATE LIMITED

Marketing Category

BULK INGREDIENT

83221-005

Substance

SODIUM PICOSULFATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2023-10-17

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2025
01 Apr
Bulk Ingredient NDC: 83221-006

Nonproprietary Name

Diclofenac Sodium

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

KREATIVE ACTIVES PRIVATE LIMITED

Marketing Category

BULK INGREDIENT

83221-006

Substance

DICLOFENAC SODIUM

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2025-04-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2024
30 Nov
Bulk Ingredient NDC: 83221-007

Nonproprietary Name

Glipizide

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

KREATIVE ACTIVES PRIVATE LIMITED

Marketing Category

BULK INGREDIENT

83221-007

Substance

GLIPIZIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2024-11-30

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2025
01 Jun
Bulk Ingredient NDC: 83221-008

Nonproprietary Name

Ferric Carboxymaltose

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

KREATIVE ACTIVES PRIVATE LIMITED

Marketing Category

BULK INGREDIENT

83221-008

Substance

FERRIC CARBOXYMALTOSE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2025-06-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

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NDC Type Breakdown
8 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).

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NDC Record Details Preview

Explore important National Drug Code information available in the records above.

NDC

83221-001

Nonproprietary Name

BISACODYL

Labeler

KREATIVE ACTIVES PRIVATE LIMITED

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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