RecallHawk

HEPARIN SODIUM

SHENZHEN TECHDOW

Summary

FDA approved HEPARIN SODIUM by SHENZHEN TECHDOW. ANDA (Generic) approval (Labeling) on 2022-02-15. INJECTABLE, INJECTION.

Details

Source

Drug Approval

External ID

ANDA202957-13

Action Date

2022-02-15

Status

Approved

Category

drug

Product Code

ANDA (Generic)

Product Description

HEPARIN SODIUM, INJECTABLE, INJECTION. Application: ANDA202957

Context & Analysis

SHENZHEN TECHDOW has 2 FDA actions in our database.

Frequently Asked Questions

How often does SHENZHEN TECHDOW have FDA actions?

SHENZHEN TECHDOW has 2 FDA actions in our database, including 0 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "ANDA202957-13" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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