United States · FDA National Drug Code directory

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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
71205-012_9c466480-174a-4ddc-a720-76e5d3911f01
Product NDC
71205-012
Form
TABLET
Composition / generic term
DEXAMETHASONE
Labeler
Proficient Rx LP
Marketing category
ANDA
Marketing start / end (source format)
20180119
Source listing expiry
20261231

Source-listed ingredients

  • DEXAMETHASONE — 1.5 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 1 BLISTER PACK in 1 CARTON (71205-012-21) / 21 TABLET in 1 BLISTER PACK · 71205-012-21

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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