Sri Krishna Pharmaceuticals
NDC Database

Sri Krishna 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 7
  • Latest Marketing Date 2025-11-01
  • Data Source FDA
  • First Marketing Date 2011-04-18
Company Overview

Company

Sri Krishna Pharmaceuticals

Country

India

Website

Visit Website

Email

vvk@srikrishnapharma.com

Social Profiles

Company Snapshot

Sri Krishna Pharmaceuticals

C-4, Industrial Area, Uppal, HYDERABAD – 500 039, Telangana

India

www.srikrishnapharma.com/ vvk@srikrishnapharma.com View on Map
NDC Records ( 7 records )
2011
18 Apr
Bulk Ingredient NDC: 66326-100

Nonproprietary Name

Acetaminophen

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Sri Krishna Pharmaceuticals Ltd. Unit I

Marketing Category

BULK INGREDIENT

66326-100

Substance

ACETAMINOPHEN

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2011-04-18

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2020
20 Jan
Bulk Ingredient NDC: 66326-101

Nonproprietary Name

DOMPERIDONE

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Sri Krishna Pharmaceuticals Ltd. Unit I

Marketing Category

BULK INGREDIENT

66326-101

Substance

DOMPERIDONE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2020-01-20

End Marketing Date

-

Listing Record Certified Through

2027-12-31

2012
01 Mar
Bulk Ingredient NDC: 66326-400

Nonproprietary Name

GLIPIZIDE

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Sri Krishna Pharmaceuticals Ltd. Unit I

Marketing Category

BULK INGREDIENT

66326-400

Substance

GLIPIZIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2012-03-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2025
01 Nov
Bulk Ingredient NDC: 66326-402

Nonproprietary Name

Glyburide

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Sri Krishna Pharmaceuticals Ltd. Unit I

Marketing Category

BULK INGREDIENT

66326-402

Substance

GLYBURIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2025-11-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2011
06 Jun
Bulk Ingredient NDC: 66326-504

Nonproprietary Name

Sodium Phenylbutyrate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Sri Krishna Pharmaceuticals Ltd. Unit I

Marketing Category

BULK INGREDIENT

66326-504

Substance

SODIUM PHENYLBUTYRATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2011-06-06

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2020
19 Jan
Bulk Ingredient NDC: 66326-809

Nonproprietary Name

Meclizine Hydrochloride

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Sri Krishna Pharmaceuticals Ltd. Unit I

Marketing Category

BULK INGREDIENT

66326-809

Substance

MECLIZINE HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2020-01-19

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2024
01 Jun
Bulk Ingredient NDC: 66326-910

Nonproprietary Name

Glipizide

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Sri Krishna Pharmaceuticals Ltd. Unit I

Marketing Category

BULK INGREDIENT

66326-910

Substance

GLIPIZIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2024-06-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

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NDC Type Breakdown
7 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

66326-100

Nonproprietary Name

Acetaminophen

Labeler

Sri Krishna Pharmaceuticals Ltd. Unit I

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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