United States · FDA National Drug Code directory
Ibuprofen PM
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
- 30142-232_46184215-a798-8ac7-e063-6294a90a0dea
- Product NDC
- 30142-232
- Form
- CAPSULE, LIQUID FILLED
- Composition / generic term
- IBUPROFEN, DIPHENHYDRAMINE HCL
- Labeler
- KROGER COMPANY
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20210824
- 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, PLASTIC in 1 CARTON (30142-232-15) / 40 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC · 30142-232-15
- 1 BOTTLE, PLASTIC in 1 CARTON (30142-232-78) / 80 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC · 30142-232-78
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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