United States · FDA National Drug Code directory

Ibuprofen and Diphenhydramine Citrate

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference: 55111-565_d2953b94-9244-2c86-ac0c-7610dd1e7963
Product NDC: 55111-565
Form: TABLET
Composition / generic term: Ibuprofen and Diphenhydramine Citrate
Labeler: Dr. Reddy's Laboratories Limited
Marketing category: ANDA
Marketing start / end (source format): 20100131
Source listing expiry: 20261231

Source-listed ingredients

IBUPROFEN — 200 mg/1
DIPHENHYDRAMINE CITRATE — 38 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

1 BOTTLE in 1 CARTON (55111-565-05) / 500 TABLET in 1 BOTTLE · 55111-565-05
1 BOTTLE in 1 CARTON (55111-565-14) / 20 TABLET in 1 BOTTLE · 55111-565-14
1 BOTTLE in 1 CARTON (55111-565-18) / 180 TABLET in 1 BOTTLE · 55111-565-18
1 BOTTLE in 1 CARTON (55111-565-30) / 30 TABLET in 1 BOTTLE · 55111-565-30
1 BOTTLE in 1 CARTON (55111-565-40) / 40 TABLET in 1 BOTTLE · 55111-565-40
1 BOTTLE in 1 CARTON (55111-565-80) / 80 TABLET in 1 BOTTLE · 55111-565-80
1 BOTTLE in 1 CARTON (55111-565-90) / 90 TABLET in 1 BOTTLE · 55111-565-90
2500 TABLET in 1 POUCH (55111-565-92) · 55111-565-92

Source and coverage

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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

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