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
- 69452-205_0f6b5911-edb2-4e3a-b121-45c609b4c60e
- Product NDC
- 69452-205
- Form
- CAPSULE, LIQUID FILLED
- Composition / generic term
- IBUPROFEN, DIPHENHYDRAMINE HCL
- Labeler
- Bionpharma Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20181101
- 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 BLISTER PACK in 1 CARTON (69452-205-04) / 6 CAPSULE, LIQUID FILLED in 1 BLISTER PACK · 69452-205-04
- 20 CAPSULE, LIQUID FILLED in 1 BOTTLE (69452-205-11) · 69452-205-11
- 40 CAPSULE, LIQUID FILLED in 1 BOTTLE (69452-205-15) · 69452-205-15
- 100 CAPSULE, LIQUID FILLED in 1 BOTTLE (69452-205-20) · 69452-205-20
- 80 CAPSULE, LIQUID FILLED in 1 BOTTLE (69452-205-78) · 69452-205-78
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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