United States · FDA National Drug Code directory
IBUPROFEN, DIPHENHYDRAMINE HCL
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
- 11822-0789_a35f6b2b-8e67-dd2d-e053-2995a90a27e1
- Product NDC
- 11822-0789
- Form
- CAPSULE, LIQUID FILLED
- Composition / generic term
- IBUPROFEN, DIPHENHYDRAMINE HCL
- Labeler
- Rite Aid Corporation
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20200415
- Source listing expiry
- 20261231
Source-listed ingredients
- IBUPROFEN — 200 mg/1
- DIPHENHYDRAMINE HYDROCHLORIDE — 25 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BOTTLE in 1 CARTON (11822-0789-4) / 40 CAPSULE, LIQUID FILLED in 1 BOTTLE · 11822-0789-4
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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