Ibuprofen And Diphenhydramine Citrate (Ibuprofen and Diphenhydramine Citrate)

Aurobindo Pharma Limited · tablet, coated · NDC 59651-692

Listed in the FDA National Drug Code directory

Ibuprofen And Diphenhydramine Citrate is a medicine made available by Aurobindo Pharma Limited, on the U.S. market since May 2022. Its listing category is "DRUG FOR FURTHER PROCESSING". Listing is not the same as FDA approval. A listing proves the product exists; it does not prove that a particular pack is genuine, so compare yours with the official description below.

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Recalls of this product

No FDA recalls are recorded for NDC 59651-692. Recalls are listed in FDA enforcement reports from 2004 onward.

Most reported side effects for ibuprofen and diphenhydramine citrateReports to the FDA Adverse Event Reporting System (FAERS), all products with this ingredient
Drug ineffective2,823 reports
Pain1,964 reports
Nausea1,806 reports
Headache1,740 reports
Fatigue1,423 reports
Dizziness1,227 reports
Vomiting1,092 reports
Anxiety1,072 reports
Drug hypersensitivity1,047 reports
Diarrhoea939 reports
Show as table
ItemValue (reports)
Drug ineffective2,823
Pain1,964
Nausea1,806
Headache1,740
Fatigue1,423
Dizziness1,227
Vomiting1,092
Anxiety1,072
Drug hypersensitivity1,047
Diarrhoea939

These counts are reports, not proof that the medicine caused the problem. Popular medicines get more reports simply because more people take them. They are useful for spotting what to watch for, not for comparing medicines.

Official listing

Brand
Ibuprofen And Diphenhydramine Citrate
Generic name
Ibuprofen and Diphenhydramine Citrate
Company
Aurobindo Pharma Limited
Form
tablet, coated
Route
—
Type
DRUG FOR FURTHER PROCESSING
Category
DRUG FOR FURTHER PROCESSING
Listing valid to
Dec 31, 2026
Product NDC
59651-692

Active ingredients

Ibuprofen
200 mg/1
Diphenhydramine Citrate
38 mg/1

Packages (1)

The last part of the NDC identifies the pack size. Your box should show one of these.

59651-692-62 30000 tablet, coated in 1 bag (59651-692-62)

Think your pack is fake?

Stop taking it, keep the pack and receipt, and show it to a pharmacist. In the U.S., report it to FDA MedWatch; elsewhere, to your national medicines regulator. How to spot a fake medicine.

Source: openFDA (U.S. Food and Drug Administration) drug directory, labels, enforcement reports and FAERS, retrieved Nov 8, 2026. The FDA notes this data should not be relied on alone for medical decisions. Not medical advice.