Shenzhen Techdow Pharmaceutical
FDA Approved Drugs

Shenzhen Techdow Pharmaceutical

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.

RX
  • Total Records 13
  • Latest Approval Date Mar 15, 2023
  • Data Source FDA
  • First Approval Date Jun 12, 2014
Company Overview

Company

Shenzhen Techdow Pharmaceutical

Country

China

Website

Visit Website

Email

sales@techdow.com

Social Profiles

Company Snapshot

Shenzhen Techdow Pharmaceutical

No.19, Gaoxinzhongyi Road, Nanshan District, Shenzhen, P. R. China 518057

China

www.techdow.com/ sales@techdow.com View on Map
FDA Approved Drug Records ( 13 records )
2023
15 Mar
RX Application: 205660

Drug Name

ENOXAPARIN SODIUM (PRESERVATIVE FREE)

Product Number

1

Dosage Form

-

Strength

30MG/0.3ML (100MG/ML)

Approval Date

2023-03-15

205660 / 1

Active Ingredient

ENOXAPARIN SODIUM

Application Number

205660

Product Number

1

Dosage Form

-

Strength

30MG/0.3ML (100MG/ML)

Approval Date

2023-03-15

Regulatory Status

RX

2023
15 Mar
RX Application: 205660

Drug Name

ENOXAPARIN SODIUM (PRESERVATIVE FREE)

Product Number

2

Dosage Form

-

Strength

40MG/0.4ML (100MG/ML)

Approval Date

2023-03-15

205660 / 2

Active Ingredient

ENOXAPARIN SODIUM

Application Number

205660

Product Number

2

Dosage Form

-

Strength

40MG/0.4ML (100MG/ML)

Approval Date

2023-03-15

Regulatory Status

RX

2023
15 Mar
RX Application: 205660

Drug Name

ENOXAPARIN SODIUM (PRESERVATIVE FREE)

Product Number

3

Dosage Form

-

Strength

60MG/0.6ML (100MG/ML)

Approval Date

2023-03-15

205660 / 3

Active Ingredient

ENOXAPARIN SODIUM

Application Number

205660

Product Number

3

Dosage Form

-

Strength

60MG/0.6ML (100MG/ML)

Approval Date

2023-03-15

Regulatory Status

RX

2023
15 Mar
RX Application: 205660

Drug Name

ENOXAPARIN SODIUM (PRESERVATIVE FREE)

Product Number

4

Dosage Form

-

Strength

80MG/0.8ML (100MG/ML)

Approval Date

2023-03-15

205660 / 4

Active Ingredient

ENOXAPARIN SODIUM

Application Number

205660

Product Number

4

Dosage Form

-

Strength

80MG/0.8ML (100MG/ML)

Approval Date

2023-03-15

Regulatory Status

RX

2023
15 Mar
RX Application: 205660

Drug Name

ENOXAPARIN SODIUM (PRESERVATIVE FREE)

Product Number

5

Dosage Form

-

Strength

100MG/ML (100MG/ML)

Approval Date

2023-03-15

205660 / 5

Active Ingredient

ENOXAPARIN SODIUM

Application Number

205660

Product Number

5

Dosage Form

-

Strength

100MG/ML (100MG/ML)

Approval Date

2023-03-15

Regulatory Status

RX

2023
15 Mar
RX Application: 205660

Drug Name

ENOXAPARIN SODIUM (PRESERVATIVE FREE)

Product Number

6

Dosage Form

-

Strength

120MG/0.8ML (150MG/ML)

Approval Date

2023-03-15

205660 / 6

Active Ingredient

ENOXAPARIN SODIUM

Application Number

205660

Product Number

6

Dosage Form

-

Strength

120MG/0.8ML (150MG/ML)

Approval Date

2023-03-15

Regulatory Status

RX

2023
15 Mar
RX Application: 205660

Drug Name

ENOXAPARIN SODIUM (PRESERVATIVE FREE)

Product Number

7

Dosage Form

-

Strength

150MG/ML (150MG/ML)

Approval Date

2023-03-15

205660 / 7

Active Ingredient

ENOXAPARIN SODIUM

Application Number

205660

Product Number

7

Dosage Form

-

Strength

150MG/ML (150MG/ML)

Approval Date

2023-03-15

Regulatory Status

RX

2014
12 Jun
RX Application: 202733

Drug Name

HEPARIN SODIUM

Product Number

1

Dosage Form

-

Strength

5,000 UNITS/ML

Approval Date

2014-06-12

202733 / 1

Active Ingredient

HEPARIN SODIUM

Application Number

202733

Product Number

1

Dosage Form

-

Strength

5,000 UNITS/ML

Approval Date

2014-06-12

Regulatory Status

RX

2014
12 Jun
RX Application: 202957

Drug Name

HEPARIN SODIUM

Product Number

1

Dosage Form

-

Strength

1,000 UNITS/ML

Approval Date

2014-06-12

202957 / 1

Active Ingredient

HEPARIN SODIUM

Application Number

202957

Product Number

1

Dosage Form

-

Strength

1,000 UNITS/ML

Approval Date

2014-06-12

Regulatory Status

RX

2014
12 Jun
RX Application: 202957

Drug Name

HEPARIN SODIUM

Product Number

2

Dosage Form

-

Strength

5,000 UNITS/ML

Approval Date

2014-06-12

202957 / 2

Active Ingredient

HEPARIN SODIUM

Application Number

202957

Product Number

2

Dosage Form

-

Strength

5,000 UNITS/ML

Approval Date

2014-06-12

Regulatory Status

RX

2014
12 Jun
RX Application: 203198

Drug Name

HEPARIN SODIUM

Product Number

1

Dosage Form

-

Strength

10,000 UNITS/ML

Approval Date

2014-06-12

203198 / 1

Active Ingredient

HEPARIN SODIUM

Application Number

203198

Product Number

1

Dosage Form

-

Strength

10,000 UNITS/ML

Approval Date

2014-06-12

Regulatory Status

RX

2014
12 Jun
RX Application: 203198

Drug Name

HEPARIN SODIUM

Product Number

2

Dosage Form

-

Strength

20,000 UNITS/ML

Approval Date

2014-06-12

203198 / 2

Active Ingredient

HEPARIN SODIUM

Application Number

203198

Product Number

2

Dosage Form

-

Strength

20,000 UNITS/ML

Approval Date

2014-06-12

Regulatory Status

RX

2014
12 Jun
RX Application: 202732

Drug Name

HEPARIN SODIUM PRESERVATIVE FREE

Product Number

1

Dosage Form

-

Strength

1,000 UNITS/ML

Approval Date

2014-06-12

202732 / 1

Active Ingredient

HEPARIN SODIUM

Application Number

202732

Product Number

1

Dosage Form

-

Strength

1,000 UNITS/ML

Approval Date

2014-06-12

Regulatory Status

RX

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Drug Status Breakdown
13 total
  • RX
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

ENOXAPARIN SODIUM (PRESERVATIVE FREE)

Application Number

205660

Product Number

1

Active Ingredient

ENOXAPARIN SODIUM

Dosage Form

-

Strength

30MG/0.3ML (100MG/ML)

FDA Approved Drug Data

Approved drug product information

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Data maintained from official sources

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