Yuhan Corporation
NDC Database

Yuhan Corporation

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 8
  • Latest Marketing Date 2025-05-26
  • Data Source FDA
  • First Marketing Date 2003-11-21
Company Overview

Company

Yuhan Corporation

Country

South Korea

Website

Visit Website

Email

shinmc@yuhan.co.kr

Social Profiles

Company Snapshot

Yuhan Corporation

74, Noryangjin-ro, Daebang-dong, Dongjak-gu, SEOUL

South Korea

eng.yuhan.co.kr/Main/ shinmc@yuhan.co.kr View on Map
NDC Records ( 8 records )
2016
28 Oct
Bulk Ingredient NDC: 66721-800

Nonproprietary Name

Velpatasvir

Dosage Form

POWDER

Strength

10 kg/10kg

Labeler

Yuhan Chemical Inc

Marketing Category

BULK INGREDIENT

66721-800

Substance

VELPATASVIR

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2016-10-28

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2019
01 Nov
Bulk Ingredient NDC: 66721-820

Nonproprietary Name

Voxilaprevir

Dosage Form

POWDER

Strength

20 kg/20kg

Labeler

Yuhan Chemical Inc

Marketing Category

BULK INGREDIENT

66721-820

Substance

VOXILAPREVIR

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2019-11-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2022
17 Aug
Bulk Ingredient NDC: 66721-830

Nonproprietary Name

Lenacapavir

Dosage Form

POWDER

Strength

20 kg/20kg

Labeler

Yuhan Chemical Inc

Marketing Category

BULK INGREDIENT

66721-830

Substance

LENACAPAVIR

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2022-08-17

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2025
26 May
Bulk Ingredient NDC: 66721-840

Nonproprietary Name

Acoramidis HCl

Dosage Form

POWDER

Strength

50 kg/50kg

Labeler

Yuhan Chemical Inc

Marketing Category

BULK INGREDIENT

66721-840

Substance

ACORAMIDIS HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2025-05-26

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2003
21 Nov
Bulk Ingredient NDC: 66721-300

Nonproprietary Name

Piperacillin

Dosage Form

POWDER

Strength

75 kg/75kg

Labeler

Yuhan Chemical Inc.

Marketing Category

BULK INGREDIENT

66721-300

Substance

PIPERACILLIN

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2003-11-21

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2005
14 Feb
Bulk Ingredient NDC: 66721-400

Nonproprietary Name

emtricitabine

Dosage Form

POWDER

Strength

60 kg/60kg

Labeler

Yuhan Chemical Inc.

Marketing Category

BULK INGREDIENT

66721-400

Substance

EMTRICITABINE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2005-02-14

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2012
24 Sep
Bulk Ingredient NDC: 66721-600

Nonproprietary Name

elvitegravir

Dosage Form

POWDER

Strength

50 kg/50kg

Labeler

Yuhan Chemical Inc.

Marketing Category

BULK INGREDIENT

66721-600

Substance

ELVITEGRAVIR

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2012-09-24

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2013
02 Dec
Bulk Ingredient NDC: 66721-700

Nonproprietary Name

ledipasvir

Dosage Form

POWDER

Strength

50 kg/50kg

Labeler

Yuhan Chemical Inc.

Marketing Category

BULK INGREDIENT

66721-700

Substance

LEDIPASVIR

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2013-12-02

End Marketing Date

-

Listing Record Certified Through

2026-12-31

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NDC Type Breakdown
8 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

66721-800

Nonproprietary Name

Velpatasvir

Labeler

Yuhan Chemical Inc

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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