RecallHawk

THEOPHYLLINE

ANNORA PHARMA

Summary

FDA approved THEOPHYLLINE by ANNORA PHARMA. ANDA (Generic) approval on 2023-09-08. TABLET, EXTENDED RELEASE, ORAL.

Details

Source

Drug Approval

External ID

ANDA217422-1

Action Date

2023-09-08

Status

Approved

Category

drug

Product Code

ANDA (Generic)

Product Description

THEOPHYLLINE, TABLET, EXTENDED RELEASE, ORAL. Application: ANDA217422

Context & Analysis

ANNORA PHARMA has 22 FDA actions in our database.

Frequently Asked Questions

How often does ANNORA PHARMA have FDA actions?

ANNORA PHARMA has 22 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 "ANDA217422-1" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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