Amoli Organics
NDC Database

Amoli 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 3
  • Latest Marketing Date 2025-09-01
  • Data Source FDA
  • First Marketing Date 2021-03-11
Company Overview

Company

Amoli Organics

Country

India

Social Profiles

Company Snapshot

Amoli Organics

407, Dalamal House, Jamnalal Bajaj Road, Nariman Point, Mumbai - 400 021, Maharashtra

India

www.amoliindia.com/ nikunj@amoliindia.com View on Map
NDC Records ( 3 records )
2021
11 Mar
Bulk Ingredient NDC: 62512-0078

Nonproprietary Name

Deferasirox

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Amoli Organics (A Division of Umedica Laboratories Pvt. Ltd.)

Marketing Category

BULK INGREDIENT

62512-0078

Substance

DEFERASIROX

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2021-03-11

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2025
01 Sep
Bulk Ingredient NDC: 62512-0084

Nonproprietary Name

Sitagliptin Phosphate Monohydrate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Amoli Organics (A Division of Umedica Laboratories Pvt. Ltd.)

Marketing Category

BULK INGREDIENT

62512-0084

Substance

SITAGLIPTIN PHOSPHATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2025-09-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2025
01 Sep
Bulk Ingredient NDC: 62512-0085

Nonproprietary Name

Sacubitril/Valsartan

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Amoli Organics (A Division of Umedica Laboratories Pvt. Ltd.)

Marketing Category

BULK INGREDIENT

62512-0085

Substance

SACUBITRIL VALSARTAN

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2025-09-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

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NDC Type Breakdown
3 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

62512-0078

Nonproprietary Name

Deferasirox

Labeler

Amoli Organics (A Division of Umedica Laboratories Pvt. Ltd.)

Dosage Form

POWDER

FDA NDC Data

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Data maintained from official sources

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NDC data is based on publicly available U.S. Food and Drug Administration (FDA) National Drug Code information.

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