Smilax Laboratories Limited
NDC Database

Smilax Laboratories 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 4
  • Latest Marketing Date 2025-07-03
  • Data Source FDA
  • First Marketing Date 2017-09-20
Company Overview

Company

Smilax Laboratories Limited

Country

India

Website

Visit Website

Email

info@smilaxlabs.com

Social Profiles

Company Snapshot

Smilax Laboratories Limited

Unit-I Plot no: 12/A, Phase - III, IDA, Jeedimetla, Hyderabad-500 055, Telangana

India

www.smilaxlabs.com/ info@smilaxlabs.com View on Map
NDC Records ( 4 records )
2017
20 Sep
Bulk Ingredient NDC: 71747-001

Nonproprietary Name

OMEPRAZOLE

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Smilax Laboratories Limited

Marketing Category

BULK INGREDIENT

71747-001

Substance

OMEPRAZOLE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2017-09-20

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2019
01 Mar
Bulk Ingredient NDC: 71747-002

Nonproprietary Name

ITRACONAZOLE

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Smilax Laboratories Limited

Marketing Category

BULK INGREDIENT

71747-002

Substance

ITRACONAZOLE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2019-03-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2022
08 Aug
Bulk Ingredient NDC: 71747-003

Nonproprietary Name

GUAIFENESIN

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Smilax Laboratories Limited

Marketing Category

BULK INGREDIENT

71747-003

Substance

GUAIFENESIN

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2022-08-08

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2025
03 Jul
Bulk Ingredient NDC: 71747-004

Nonproprietary Name

Esomeprazole Magnesium

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Smilax Laboratories Limited

Marketing Category

BULK INGREDIENT

71747-004

Substance

ESOMEPRAZOLE MAGNESIUM

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2025-07-03

End Marketing Date

-

Listing Record Certified Through

2026-12-31

Related Databases
  • FDA Inspections
    2 View
  • EDQM CEP
    9 View
  • KDMF
    0 View
  • Japan DMF
    0 View
  • Eudra GMP
    0 View
  • NDC Database
    4 View
  • FDA Approved Drugs Database
    0 View
  • Drug Prices in Switzerland
    0 View
NDC Type Breakdown
4 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

71747-001

Nonproprietary Name

OMEPRAZOLE

Labeler

Smilax Laboratories 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.

Create a New Buying Request

Fields marked with * are mandatory.

Please enter quantity.
Please select a unit.
Please select quality standard.
Please select request type.
Please provide product specifications.
Please enter additional details.
Please select shipping preference.
Notice: By submitting this buying request, the provided product details and requirements may be published publicly on our marketplace.
Login to Submit