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General MedicationsORALGeneric

ABSORICA LD

ISOTRETINOIN

Standard Dose
28MG
Max Dose
Refer to approved labeling
Primary Use
Review priority: N/A Marketing status: Discontinued
Summary

Approval overview ABSORICA LD is listed in Drugs@FDA under application 211913 (NDA).

Review priority: N/A Marketing status: Discontinued Active ingredient ISOTRETINOIN Form and strength CAPSULE;ORAL - 28MG Sponsor SUN PHARM Submission history Latest submission status date: 2026-02-09 00:00:00.

Structured Monograph

Clinical summary

Approval overview ABSORICA LD is listed in Drugs@FDA under application 211913 (NDA). Review priority: N/A Marketing status: Discontinued Active ingredient ISOTRETINOIN Form and strength CAPSULE;ORAL - 28MG Sponsor SUN PHARM Submission history Latest submission status date: 2026-02-09 00:00:00. Submission type: SUPPL.

Monitoring

  • • Marketing status: Discontinued
  • • Review priority: N/A

Interaction Notes

  • No interaction notes stored yet.