United States · FDA National Drug Code directory
Roflumilast
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
- 72205-201_b56e7d3f-9930-43fa-baf4-63f9cee750f2
- Product NDC
- 72205-201
- Form
- TABLET
- Composition / generic term
- Roflumilast
- Labeler
- Novadoz Pharmaceuticals LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20220907
- Source listing expiry
- 20261231
Source-listed ingredients
- ROFLUMILAST — 250 ug/1
These values do not establish equivalence or a dose recommendation.
Packages
- 2 BLISTER PACK in 1 CARTON (72205-201-24) / 10 TABLET in 1 BLISTER PACK (72205-201-11) · 72205-201-24
- 30 TABLET in 1 BOTTLE (72205-201-30) · 72205-201-30
- 2 BLISTER PACK in 1 CARTON (72205-201-32) / 14 TABLET in 1 BLISTER PACK (72205-201-13) · 72205-201-32
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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