United States · FDA National Drug Code directory
Ibuprofen 200 mg and Diphenhydramine Citrate 38 mg
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
- 63548-0197_fbc47d79-348d-436e-ae3f-364d76f58e49
- Product NDC
- 63548-0197
- Form
- TABLET
- Composition / generic term
- Ibuprofen, Diphenhydramine Citrate
- Labeler
- PLD Acquisitions LLC DBA Avma Pharma Solutions
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20240411
- 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, PLASTIC in 1 BOX (63548-0197-2) / 20 TABLET in 1 BOTTLE, PLASTIC · 63548-0197-2
- 300 TABLET in 1 BOTTLE, PLASTIC (63548-0197-3) · 63548-0197-3
- 8 TABLET in 1 BOTTLE, PLASTIC (63548-0197-8) · 63548-0197-8
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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