Sunshine Lake Pharma Co., Ltd. Unclassified
FDA Approved Drugs

Sunshine Lake Pharma Co., Ltd. Unclassified

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.

Unclassified
  • Total Records 5
  • Latest Approval Date -
  • Data Source FDA
  • First Approval Date -
All
77
View
Unclassified
5
View
Discontinued
11
View
RX
61
View
Company Overview

Company

Sunshine Lake Pharma Co., Ltd. Unclassified

Country

China

Website

Visit Website

Email

sales@hecpharm.com

Social Profiles

Company Snapshot

Sunshine Lake Pharma Co., Ltd. Unclassified

HEC Pharm Group , Dong Yang Guang Park, Shangsha, Chang’an, Dongguan, Guangdong, 523871, China

China

www.hecpharm.com/ sales@hecpharm.com View on Map
FDA Approved Drug Records ( 5 records )
-
Unclassified Application: 209944

Drug Name

APIXABAN

Product Number

1

Dosage Form

-

Strength

2.GMG

Approval Date

-

209944 / 1

Active Ingredient

APIXABAN

Application Number

209944

Product Number

1

Dosage Form

-

Strength

2.GMG

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 209944

Drug Name

APIXABAN

Product Number

2

Dosage Form

-

Strength

5MG

Approval Date

-

209944 / 2

Active Ingredient

APIXABAN

Application Number

209944

Product Number

2

Dosage Form

-

Strength

5MG

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 761412

Drug Name

LANGLARA

Product Number

1

Dosage Form

-

Strength

100UNITS/ML

Approval Date

-

761412 / 1

Active Ingredient

INSULIN GLARGINE-ALDY

Application Number

761412

Product Number

1

Dosage Form

-

Strength

100UNITS/ML

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 216757

Drug Name

MIRABEGRON

Product Number

2

Dosage Form

-

Strength

25MG

Approval Date

-

216757 / 2

Active Ingredient

MIRABEGRON

Application Number

216757

Product Number

2

Dosage Form

-

Strength

25MG

Approval Date

-

Regulatory Status

Unclassified

-
Unclassified Application: 213845

Drug Name

TENOFOVIR ALAFENAMIDE

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

-

213845 / 1

Active Ingredient

TENOFOVIR ALAFENAMIDE

Application Number

213845

Product Number

1

Dosage Form

-

Strength

25MG

Approval Date

-

Regulatory Status

Unclassified

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Drug Status Breakdown
5 total
  • Unclassified
Official Source

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

Visit FDA Orange Book
FDA Approved Drug Record Details Preview

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

Drug Name

APIXABAN

Application Number

209944

Product Number

1

Active Ingredient

APIXABAN

Dosage Form

-

Strength

2.GMG

FDA Approved Drug Data

Approved drug product information

Regular Updates

Data maintained from official sources

Structured Database

Searchable pharmaceutical data

Reliable Data

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