Spil Discontinued
FDA Approved Drugs

Spil Discontinued

FDA Approved Drugs Database

FDA approved drug product records including application numbers, product numbers, drug names, active ingredients, dosage forms, strengths, approval dates and regulatory status.

Discontinued
  • Total Records 6
  • Latest Approval Date Feb 28, 2022
  • Data Source FDA
  • First Approval Date Jul 20, 2018
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Company Overview

Company

Spil Discontinued

Country

Taiwan

Social Profiles

Company Snapshot

Spil Discontinued

No. 123, Sec. 3, Da Fong Rd., Tantzu, Taichung 427

Taiwan

www.spil.com.tw/ info@spil.com.tw View on Map
FDA Approved Drug Records ( 6 records )
2022
28 Feb
Discontinued Application: 216018

Drug Name

ASPRUZYO SPRINKLE

Product Number

1

Dosage Form

-

Strength

500MG

Approval Date

2022-02-28

216018 / 1

Active Ingredient

RANOLAZINE

Application Number

216018

Product Number

1

Dosage Form

-

Strength

500MG

Approval Date

2022-02-28

Regulatory Status

Discontinued

2022
28 Feb
Discontinued Application: 216018

Drug Name

ASPRUZYO SPRINKLE

Product Number

2

Dosage Form

-

Strength

1GM

Approval Date

2022-02-28

216018 / 2

Active Ingredient

RANOLAZINE

Application Number

216018

Product Number

2

Dosage Form

-

Strength

1GM

Approval Date

2022-02-28

Regulatory Status

Discontinued

2019
16 Apr
Discontinued Application: 210838

Drug Name

NIFEDIPINE

Product Number

1

Dosage Form

-

Strength

30MG

Approval Date

2019-04-16

210838 / 1

Active Ingredient

NIFEDIPINE

Application Number

210838

Product Number

1

Dosage Form

-

Strength

30MG

Approval Date

2019-04-16

Regulatory Status

Discontinued

2019
16 Apr
Discontinued Application: 210838

Drug Name

NIFEDIPINE

Product Number

2

Dosage Form

-

Strength

60MG

Approval Date

2019-04-16

210838 / 2

Active Ingredient

NIFEDIPINE

Application Number

210838

Product Number

2

Dosage Form

-

Strength

60MG

Approval Date

2019-04-16

Regulatory Status

Discontinued

2019
16 Apr
Discontinued Application: 210838

Drug Name

NIFEDIPINE

Product Number

3

Dosage Form

-

Strength

90MG

Approval Date

2019-04-16

210838 / 3

Active Ingredient

NIFEDIPINE

Application Number

210838

Product Number

3

Dosage Form

-

Strength

90MG

Approval Date

2019-04-16

Regulatory Status

Discontinued

2018
20 Jul
Discontinued Application: 210593

Drug Name

OMEPRAZOLE MAGNESIUM

Product Number

1

Dosage Form

-

Strength

EQ 20MG BASE

Approval Date

2018-07-20

210593 / 1

Active Ingredient

OMEPRAZOLE MAGNESIUM

Application Number

210593

Product Number

1

Dosage Form

-

Strength

EQ 20MG BASE

Approval Date

2018-07-20

Regulatory Status

Discontinued

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Drug Status Breakdown
6 total
  • Discontinued
Official Source

FDA approved drug data is based on publicly available U.S. Food and Drug Administration Orange Book information.

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FDA Approved Drug Record Details Preview

Explore important FDA approved drug information available in the records above.

Drug Name

ASPRUZYO SPRINKLE

Application Number

216018

Product Number

1

Active Ingredient

RANOLAZINE

Dosage Form

-

Strength

500MG

FDA Approved Drug Data

Approved drug product information

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Data maintained from official sources

Structured Database

Searchable pharmaceutical data

Reliable Data

Organized FDA drug records

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