Zhejiang Ruibang Laboratories
NDC Database

Zhejiang Ruibang Laboratories

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 2021-04-05
  • Data Source FDA
  • First Marketing Date 2003-01-01
Company Overview

Company

Zhejiang Ruibang Laboratories

Country

China

Website

Email

rb@ruibang.cn

Social Profiles

Company Snapshot

Zhejiang Ruibang Laboratories

No.578 Binhai Ten Road, Economic and Technological Development Zone,Wenzhou,P.R.China

China

rb@ruibang.cn View on Map
NDC Records ( 4 records )
2014
27 Feb
Bulk Ingredient NDC: 66507-0001

Nonproprietary Name

Cyclosporine

Dosage Form

POWDER

Strength

1 g/g

Labeler

Zhejiang Ruibang Laboratories

Marketing Category

BULK INGREDIENT

66507-0001

Substance

CYCLOSPORINE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2014-02-27

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2021
05 Apr
Bulk Ingredient NDC: 66507-0002

Nonproprietary Name

Calcium Gluconate for Injection

Dosage Form

GRANULE

Strength

1 kg/kg

Labeler

Zhejiang Ruibang Laboratories

Marketing Category

BULK INGREDIENT

66507-0002

Substance

CALCIUM GLUCONATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2021-04-05

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2017
04 Dec
Bulk Ingredient NDC: 66507-7011

Nonproprietary Name

Thiostrepton

Dosage Form

POWDER

Strength

0.5 kg/.5kg

Labeler

Zhejiang Ruibang Laboratories

Marketing Category

BULK INGREDIENT

66507-7011

Substance

THIOSTREPTON

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2017-12-04

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2003
01 Jan
Bulk Ingredient NDC: 66507-7011

Nonproprietary Name

Thiostrepton

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Zhejiang Ruibang Laboratories

Marketing Category

BULK INGREDIENT

66507-7011

Substance

THIOSTREPTON

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2003-01-01

End Marketing Date

-

Listing Record Certified Through

2027-12-31

Related Databases
  • FDA Inspections
    1 View
  • EDQM CEP
    2 View
  • KDMF
    0 View
  • Japan DMF
    1 View
  • Eudra GMP
    0 View
  • NDC Database
    4 View
  • FDA Approved Drugs Database
    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

66507-0001

Nonproprietary Name

Cyclosporine

Labeler

Zhejiang Ruibang Laboratories

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