Maithili Life Sciences
NDC Database

Maithili Life Sciences

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 11
  • Latest Marketing Date 2026-01-01
  • Data Source FDA
  • First Marketing Date 2021-07-10
Company Overview

Company

Maithili Life Sciences

Country

India

Website

Visit Website

Email

info@maithililifesdences.com

Social Profiles

LinkedIn
Company Snapshot

Maithili Life Sciences

Plot # 146A, Phase - II,Road No - 16, IDA MALLAPUR, HYDERABAD

India

maithililifesciences.com/ info@maithililifesdences.com View on Map
NDC Records ( 11 records )
2021
10 Jul
Bulk Ingredient NDC: 82053-001

Nonproprietary Name

Isoxsuprine Hydrochloride

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Maithili Life Sciences Private Limited

Marketing Category

BULK INGREDIENT

82053-001

Substance

ISOXSUPRINE HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2021-07-10

End Marketing Date

-

Listing Record Certified Through

2027-12-31

2022
16 May
Bulk Ingredient NDC: 82053-002

Nonproprietary Name

Trazodone Hydrochloride

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Maithili Life Sciences Private Limited

Marketing Category

BULK INGREDIENT

82053-002

Substance

TRAZODONE HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2022-05-16

End Marketing Date

-

Listing Record Certified Through

2027-12-31

2022
10 May
Bulk Ingredient NDC: 82053-003

Nonproprietary Name

TadalafilUSP

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Maithili Life Sciences Private Limited

Marketing Category

BULK INGREDIENT

82053-003

Substance

TADALAFIL

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2022-05-10

End Marketing Date

-

Listing Record Certified Through

2027-12-31

2022
10 May
Bulk Ingredient NDC: 82053-003

Nonproprietary Name

TadalafilUSP

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Maithili Life Sciences Private Limited

Marketing Category

BULK INGREDIENT

82053-003

Substance

TADALAFIL

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2022-05-10

End Marketing Date

-

Listing Record Certified Through

2027-12-31

2022
10 Apr
Bulk Ingredient NDC: 82053-004

Nonproprietary Name

DAPOXETINE HYDROCHLORIDE

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Maithili Life Sciences Private Limited

Marketing Category

BULK INGREDIENT

82053-004

Substance

DAPOXETINE HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2022-04-10

End Marketing Date

-

Listing Record Certified Through

2027-12-31

2025
18 Apr
Bulk Ingredient NDC: 82053-005

Nonproprietary Name

VardenafilHydrochlorideTrihydrateUSP

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Maithili Life Sciences Private Limited

Marketing Category

BULK INGREDIENT

82053-005

Substance

VARDENAFIL HYDROCHLORIDE TRIHYDRATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2025-04-18

End Marketing Date

-

Listing Record Certified Through

2027-12-31

2025
18 Apr
Bulk Ingredient NDC: 82053-005

Nonproprietary Name

VardenafilHydrochlorideTrihydrateUSP

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Maithili Life Sciences Private Limited

Marketing Category

BULK INGREDIENT

82053-005

Substance

VARDENAFIL HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2025-04-18

End Marketing Date

-

Listing Record Certified Through

2027-12-31

2025
19 Jun
Bulk Ingredient NDC: 82053-006

Nonproprietary Name

Minoxidil

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Maithili Life Sciences Private Limited

Marketing Category

BULK INGREDIENT

82053-006

Substance

MINOXIDIL

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2025-06-19

End Marketing Date

-

Listing Record Certified Through

2027-12-31

2025
19 Jun
Bulk Ingredient NDC: 82053-006

Nonproprietary Name

Minoxidil

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Maithili Life Sciences Private Limited

Marketing Category

BULK INGREDIENT

82053-006

Substance

MINOXIDIL

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2025-06-19

End Marketing Date

-

Listing Record Certified Through

2027-12-31

2025
19 Jun
Bulk Ingredient NDC: 82053-006

Nonproprietary Name

Minoxidil

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Maithili Life Sciences Private Limited

Marketing Category

BULK INGREDIENT

82053-006

Substance

MINOXIDIL

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2025-06-19

End Marketing Date

-

Listing Record Certified Through

2027-12-31

2026
01 Jan
Bulk Ingredient NDC: 82053-007

Nonproprietary Name

Sildenafil Citrate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Maithili Life Sciences Private Limited

Marketing Category

BULK INGREDIENT

82053-007

Substance

SILDENAFIL CITRATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2026-01-01

End Marketing Date

-

Listing Record Certified Through

2027-12-31

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NDC Type Breakdown
11 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

82053-001

Nonproprietary Name

Isoxsuprine Hydrochloride

Labeler

Maithili Life Sciences 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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