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Isotretinoin

NDC 70710-1023 · HUMAN PRESCRIPTION DRUG · CAPSULE

Labeler / ManufacturerZydus Pharmaceuticals USA Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA211568
Dosage form / routeCAPSULE · ORAL
Active ingredientsISOTRETINOIN (20 mg/1)
Marketing started20230912
Package count2

External sources

Source: openFDA. Public-domain (CC0).