Delta Synthetic Co. Ltd Bulk Ingredient
NDC Database

Delta Synthetic Co. Ltd Bulk Ingredient

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 3
  • Latest Marketing Date 2002-06-12
  • Data Source FDA
  • First Marketing Date 1982-01-01
All
4
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Bulk Ingredient
3
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Drug for Further Processing
1
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Company Overview

Company

Delta Synthetic Co. Ltd Bulk Ingredient

Country

Taiwan

Website

Visit Website

Email

deltas@deltas.com.tw

Social Profiles

Company Snapshot

Delta Synthetic Co. Ltd Bulk Ingredient

15, Minsheng St., Tucheng Dist., New Taipei City 23679

Taiwan

www.deltas.com.tw/docs/lookupe.htm deltas@deltas.com.tw View on Map
NDC Records ( 3 records )
2002
12 Jun
Bulk Ingredient NDC: 60203-1001

Nonproprietary Name

Guaifenesin

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Delta Synthetic Co. Ltd

Marketing Category

BULK INGREDIENT

60203-1001

Substance

GUAIFENESIN

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2002-06-12

End Marketing Date

-

Listing Record Certified Through

2026-12-31

1982
01 Jan
Bulk Ingredient NDC: 60203-1002

Nonproprietary Name

Lidocaine

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Delta Synthetic Co. Ltd

Marketing Category

BULK INGREDIENT

60203-1002

Substance

LIDOCAINE HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

1982-01-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

1982
01 Jan
Bulk Ingredient NDC: 60203-1003

Nonproprietary Name

Lidocaine

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Delta Synthetic Co. Ltd

Marketing Category

BULK INGREDIENT

60203-1003

Substance

LIDOCAINE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

1982-01-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

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NDC Type Breakdown
3 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

60203-1001

Nonproprietary Name

Guaifenesin

Labeler

Delta Synthetic Co. Ltd

Dosage Form

POWDER

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Data maintained from official sources

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NDC data is based on publicly available U.S. Food and Drug Administration (FDA) National Drug Code information.

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