United States · FDA National Drug Code directory
Pain Relief Acetaminophen PM Extra Strength
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
- 11822-2350_c6e9a2de-8b16-4dbf-84f7-beef05feab78
- Product NDC
- 11822-2350
- Form
- TABLET, FILM COATED
- Composition / generic term
- Acetaminophen and Diphenhydramine HCl
- Labeler
- Rite Aid Corporation
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start / end (source format)
- 19940515
- Source listing expiry
- 20271231
Source-listed ingredients
- ACETAMINOPHEN — 500 mg/1
- DIPHENHYDRAMINE HYDROCHLORIDE — 25 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BOTTLE, PLASTIC in 1 CARTON (11822-2350-2) / 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC · 11822-2350-2
- 1 BOTTLE, PLASTIC in 1 CARTON (11822-2350-5) / 50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC · 11822-2350-5
- 300 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (11822-2350-7) · 11822-2350-7
- 1 BOTTLE, PLASTIC in 1 CARTON (11822-2350-8) / 24 TABLET, FILM COATED in 1 BOTTLE, PLASTIC · 11822-2350-8
- 1 BOTTLE, PLASTIC in 1 CARTON (11822-2350-9) / 150 TABLET, FILM COATED in 1 BOTTLE, PLASTIC · 11822-2350-9
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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