United States · FDA National Drug Code directory
Isotretinoin
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
- 68308-571_66d6a601-cb08-4662-a043-537a6f8d935b
- Product NDC
- 68308-571
- Form
- CAPSULE, LIQUID FILLED
- Composition / generic term
- Isotretinoin
- Labeler
- Mayne Pharma
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20210921
- Source listing expiry
- 20261231
Source-listed ingredients
- ISOTRETINOIN — 20 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 3 BLISTER PACK in 1 BOX (68308-571-30) / 10 CAPSULE, LIQUID FILLED in 1 BLISTER PACK (68308-571-01) · 68308-571-30
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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