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
- 21130-228_09fc3572-d282-478d-ba22-70690f615e65
- Product NDC
- 21130-228
- Form
- TABLET, COATED
- Composition / generic term
- Ibuprofen and Diphenhydramine Citrate
- Labeler
- Better Living Brands, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20231115
- 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 (21130-228-12) / 40 TABLET, COATED in 1 BOTTLE · 21130-228-12
- 1 BOTTLE in 1 CARTON (21130-228-18) / 80 TABLET, COATED in 1 BOTTLE · 21130-228-18
- 1 BOTTLE in 1 CARTON (21130-228-23) / 120 TABLET, COATED in 1 BOTTLE · 21130-228-23
- 1 BOTTLE in 1 CARTON (21130-228-73) / 20 TABLET, COATED in 1 BOTTLE · 21130-228-73
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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