United States · FDA National Drug Code directory
Feverall Jr. 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
- 51672-2116_5a99e46d-4983-579f-e063-6394a90a40db
- Product NDC
- 51672-2116
- Form
- SUPPOSITORY
- Composition / generic term
- Acetaminophen
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Marketing category
- NDA
- Marketing start / end (source format)
- 20131212
- Source listing expiry
- 20271231
Source-listed ingredients
- ACETAMINOPHEN — 325 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 6 BLISTER PACK in 1 CARTON (51672-2116-2) / 1 SUPPOSITORY in 1 BLISTER PACK (51672-2116-0) · 51672-2116-2
- 50 BLISTER PACK in 1 CARTON (51672-2116-4) / 1 SUPPOSITORY in 1 BLISTER PACK (51672-2116-0) · 51672-2116-4
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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