RecallHawk

RISEDRONATE SODIUM

SUN PHARM

Summary

FDA approved RISEDRONATE SODIUM by SUN PHARM. ANDA (Generic) approval (Labeling) on 2024-01-08. TABLET, ORAL.

Details

Source

Drug Approval

External ID

ANDA090886-11

Action Date

2024-01-08

Status

Approved

Category

drug

Product Code

ANDA (Generic)

Product Description

RISEDRONATE SODIUM, TABLET, ORAL. Application: ANDA090886

Company

Context & Analysis

SUN PHARM has 48 FDA actions in our database.

Frequently Asked Questions

How often does SUN PHARM have FDA actions?

SUN PHARM has 48 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 "ANDA090886-11" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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