Details for New Drug Application (NDA): 212333
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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 212333
Tradename: | ISOTRETINOIN |
Applicant: | Upsher Smith Labs |
Ingredient: | isotretinoin |
Patents: | 0 |
Suppliers and Packaging for NDA: 212333
Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
---|---|---|---|---|---|---|---|---|
ISOTRETINOIN | isotretinoin | CAPSULE;ORAL | 212333 | ANDA | Upsher-Smith Laboratories, LLC | 0245-0570 | 0245-0570-01 | 3 BLISTER PACK in 1 BOX (0245-0570-01) / 10 CAPSULE, LIQUID FILLED in 1 BLISTER PACK (0245-0570-89) |
ISOTRETINOIN | isotretinoin | CAPSULE;ORAL | 212333 | ANDA | Upsher-Smith Laboratories, LLC | 0245-0571 | 0245-0571-01 | 3 BLISTER PACK in 1 BOX (0245-0571-01) / 10 CAPSULE, LIQUID FILLED in 1 BLISTER PACK (0245-0571-89) |
Profile for product number 001
Active Rx/OTC/Discontinued: | RX | Dosage: | CAPSULE;ORAL | Strength | 10MG | ||||
Approval Date: | Sep 21, 2021 | TE: | AB2 | RLD: | No |
Profile for product number 002
Active Rx/OTC/Discontinued: | RX | Dosage: | CAPSULE;ORAL | Strength | 20MG | ||||
Approval Date: | Sep 21, 2021 | TE: | AB2 | RLD: | No |
Profile for product number 003
Active Rx/OTC/Discontinued: | RX | Dosage: | CAPSULE;ORAL | Strength | 30MG | ||||
Approval Date: | Sep 21, 2021 | TE: | AB2 | RLD: | No |
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