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Last Updated: April 28, 2024

Details for New Drug Application (NDA): 211568


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NDA 211568 describes ISOTRETINOIN, which is a drug marketed by Actavis Labs Fl, Amneal Pharms Ny, Aurobindo Pharma, Upsher Smith Labs, and Zydus Pharms, and is included in six NDAs. It is available from seven suppliers. Additional details are available on the ISOTRETINOIN profile page.

The generic ingredient in ISOTRETINOIN is isotretinoin. There are thirteen drug master file entries for this compound. Twelve suppliers are listed for this compound. Additional details are available on the isotretinoin profile page.
Summary for 211568
Tradename:ISOTRETINOIN
Applicant:Zydus Pharms
Ingredient:isotretinoin
Patents:0
Formulation / Manufacturing:see details
Pharmacology for NDA: 211568
Medical Subject Heading (MeSH) Categories for 211568
Suppliers and Packaging for NDA: 211568
Tradename Generic Name Dosage NDA Application Type Supplier National Drug Code Package Code Package
ISOTRETINOIN isotretinoin CAPSULE;ORAL 211568 ANDA Zydus Pharmaceuticals USA Inc. 70710-1022 70710-1022-4 10 BLISTER PACK in 1 CARTON (70710-1022-4) / 10 CAPSULE in 1 BLISTER PACK
ISOTRETINOIN isotretinoin CAPSULE;ORAL 211568 ANDA Zydus Pharmaceuticals USA Inc. 70710-1022 70710-1022-8 3 BLISTER PACK in 1 CARTON (70710-1022-8) / 10 CAPSULE in 1 BLISTER PACK

Profile for product number 001

Active Rx/OTC/Discontinued:RXDosage:CAPSULE;ORALStrength10MG
Approval Date:Aug 29, 2023TE:AB1RLD:No

Profile for product number 002

Active Rx/OTC/Discontinued:RXDosage:CAPSULE;ORALStrength20MG
Approval Date:Aug 29, 2023TE:AB1RLD:No

Profile for product number 003

Active Rx/OTC/Discontinued:RXDosage:CAPSULE;ORALStrength30MG
Approval Date:Aug 29, 2023TE:AB1RLD:No

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