Megafine Pharma (P) Limited
NDC Database

Megafine Pharma (P) Limited

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 2026-01-02
  • Data Source FDA
  • First Marketing Date 2010-07-19
Company Overview

Company

Megafine Pharma (P) Limited

Country

India

Website

Visit Website

Email

info@megafine.in

Social Profiles

LinkedIn X / Twitter
Company Snapshot

Megafine Pharma (P) Limited

Sethna 4th floor, 55 Maharshi Karve Road, Marine Lines, Mumbai – 400 002 Maharashtra

India

megafine.in/ info@megafine.in View on Map
NDC Records ( 3 records )
2026
02 Jan
Bulk Ingredient NDC: 22665-0001

Nonproprietary Name

Mirtazapine Anhydrous

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Megafine Pharma (P) limited

Marketing Category

BULK INGREDIENT

22665-0001

Substance

MIRTAZAPINE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2026-01-02

End Marketing Date

-

Listing Record Certified Through

2027-12-31

2010
19 Jul
Bulk Ingredient NDC: 22665-0002

Nonproprietary Name

Pyrantel Pamoate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Megafine Pharma (P) Limited

Marketing Category

BULK INGREDIENT

22665-0002

Substance

PYRANTEL PAMOATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2010-07-19

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2011
24 Mar
Bulk Ingredient NDC: 22665-0015

Nonproprietary Name

Memantine Hydrochloride

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Megafine Pharma (P) Limited

Marketing Category

BULK INGREDIENT

22665-0015

Substance

MEMANTINE HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2011-03-24

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

22665-0001

Nonproprietary Name

Mirtazapine Anhydrous

Labeler

Megafine Pharma (P) limited

Dosage Form

POWDER

FDA NDC Data

National Drug Code information

Regular Updates

Data maintained from official sources

Structured Database

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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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