Details for New Drug Application (NDA): 212722
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The generic ingredient in PIRFENIDONE is pirfenidone. There are twenty-three drug master file entries for this compound. Twenty-one suppliers are listed for this compound. Additional details are available on the pirfenidone profile page.
Summary for 212722
Tradename: | PIRFENIDONE |
Applicant: | Laurus |
Ingredient: | pirfenidone |
Patents: | 0 |
Suppliers and Packaging for NDA: 212722
Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
---|---|---|---|---|---|---|---|---|
PIRFENIDONE | pirfenidone | TABLET;ORAL | 212722 | ANDA | Laurus Labs Limited | 42385-924 | 42385-924-99 | 3 BOTTLE in 1 CARTON (42385-924-99) / 90 TABLET, FILM COATED in 1 BOTTLE |
PIRFENIDONE | pirfenidone | TABLET;ORAL | 212722 | ANDA | Laurus Labs Limited | 42385-925 | 42385-925-90 | 90 TABLET, FILM COATED in 1 BOTTLE (42385-925-90) |
Profile for product number 001
Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 267MG | ||||
Approval Date: | Jul 19, 2022 | TE: | AB | RLD: | No |
Profile for product number 002
Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 534MG | ||||
Approval Date: | Jul 19, 2022 | TE: | AB | RLD: | No |
Profile for product number 003
Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 801MG | ||||
Approval Date: | Jul 19, 2022 | TE: | AB | RLD: | No |
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