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IBUPROFEN 200 MG AND DIPHENHYDRAMINE CITRATE 38 MG (IBUPROFEN, DIPHENHYDRAMINE CITRATE)

PLD ACQUISITIONS LLC

Summary

FDA approved IBUPROFEN 200 MG AND DIPHENHYDRAMINE CITRATE 38 MG (IBUPROFEN, DIPHENHYDRAMINE CITRATE) by PLD ACQUISITIONS LLC. ANDA (Generic) approval on 2024-04-11. TABLET, ORAL.

Details

Source

Drug Approval

External ID

ANDA211404-1

Action Date

2024-04-11

Status

Approved

Category

drug

Product Code

ANDA (Generic)

Product Description

IBUPROFEN 200 MG AND DIPHENHYDRAMINE CITRATE 38 MG (generic: IBUPROFEN, DIPHENHYDRAMINE CITRATE), TABLET, ORAL. Application: ANDA211404

Context & Analysis

Frequently Asked Questions

How often does PLD ACQUISITIONS LLC have FDA actions?

This is the only FDA action we have on record for PLD ACQUISITIONS LLC in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "ANDA211404-1" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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