United States · FDA National Drug Code directory

FENOPROFEN CALCIUM

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: 71993-308_14a4aa5b-30ff-8ad7-e063-6294a90a889e
Product NDC: 71993-308
Form: CAPSULE
Composition / generic term: FENOPROFEN CALCIUM
Labeler: Atland Pharmaceuticals, LLC
Marketing category: ANDA
Marketing start / end (source format): 20240326
Source listing expiry: 20261231

Source-listed ingredients

FENOPROFEN CALCIUM — 400 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

90 CAPSULE in 1 BOTTLE (71993-308-90) · 71993-308-90

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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