Home Applications 212099 Application 212099
Type NDA
Sponsor BAYER HEALTHCARE Application Products# Product, Drug, Ingredient table Product Drug Ingredient Form Strength Reference drug Reference standard 001 NUBEQA DAROLUTAMIDE TABLET;ORAL 300MG Yes Yes
Source provenance: Browse the complete Orange Book source catalog · source snapshot 44 .
Orange Book products# Current product rows page 1 of 1 · 1 matching rows.
Application-product, Trade name, Ingredient table Application-product Trade name Ingredient Strength Dosage form / route TE codes RLD / RS Approval date N212099-001 NUBEQA DAROLUTAMIDE 300MG TABLET / ORAL RLD, RS 2019-07-30
Orange Book patents# Current patent rows page 1 of 1 · 17 matching rows.
Application-product, Patent, Expiration table Application-product Patent Expiration Use code Coverage / status Submission date N212099-001 10711013 2030-10-27 Drug substance, Drug product 2020-08-11 N212099-001 11046713 2030-10-27 Drug substance 2021-07-28 N212099-001 9657003 2030-10-27 U-4208 Drug substance, Drug product 2019-08-27 N212099-001 9657003 2030-10-27 U-4209 Drug substance, Drug product 2019-08-27 N212099-001 9657003 2030-10-27 U-4210 Drug substance, Drug product 2019-08-27 N212099-001 8975254 2033-03-25 U-4208 Drug substance, Drug product 2019-08-27 N212099-001 8975254 2033-03-25 U-4209 Drug substance, Drug product 2019-08-27 N212099-001 8975254 2033-03-25 U-4210 Drug substance, Drug product 2019-08-27 N212099-001 10010530 2036-01-28 Drug substance 2019-08-27 N212099-001 10383853 2036-01-28 Drug substance 2019-08-27 N212099-001 10835515 2036-01-28 U-2605 Drug product 2020-12-11 N212099-001 10835515 2036-01-28 U-4208 Drug product 2020-12-11 N212099-001 10835515 2036-01-28 U-4209 Drug product 2020-12-11 N212099-001 10835515 2036-01-28 U-4210 Drug product 2020-12-11 N212099-001 11168058 2038-02-27 Drug substance, Drug product 2022-01-27 N212099-001 12611397 2040-07-02 Drug product 2026-05-15 N212099-001 12329742 2042-06-17 Drug product 2025-07-02
Orange Book exclusivity# Current exclusivity rows page 1 of 1 · 1 matching rows.
Application-product, Exclusivity code, Expiration table Application-product Exclusivity code Expiration N212099-001 I-971 2028-06-03
Observed Orange Book product history# Observed FDA ZIP history: Each table is queried independently by exact application/product key from successfully parsed Orange Book snapshots. Capture times identify archived source observations; absence or a change between snapshots is not inferred. FDA publication files that were not recoverable as structured ZIP data are not represented as states.
Product history page 2 of 2 · 43 observed states.
Captured, Edition, Application-product table Captured Edition Application-product Trade name Strength Dosage form / route Product TE source text RLD / RS Approval date Source SHA-256 2022-09-29 23:25 UTC 2022-09 N212099-001 NUBEQA 300MG TABLET / ORAL RLD, RS 2019-07-30 e64feba35796…2022-07-09 03:26 UTC · 3 captures of this ZIP 2022-07 N212099-001 NUBEQA 300MG TABLET / ORAL RLD, RS 2019-07-30 cb3db0bc1861…2026-07-26 02:55 UTC · 3 captures of this ZIP 2026-06 N212099-001 NUBEQA 300MG TABLET / ORAL RLD, RS 2019-07-30 a50c72e98297…
Observed Orange Book patent history# Patent history page 1 of 10 · 381 observed states.
Captured, Edition, Application-product table Captured Edition Application-product Patent Expiration Use code Coverage / status Submission date Source SHA-256 2026-10-15 13:18:30 2026-09 N212099-001 10711013 2030-10-27 Drug substance, Drug product 2020-08-11 c2088c7a36db…2026-10-15 13:18:30 2026-09 N212099-001 11046713 2030-10-27 Drug substance 2021-07-28 c2088c7a36db…2026-10-15 13:18:30 2026-09 N212099-001 9657003 2030-10-27 U-4209 Drug substance, Drug product 2019-08-27 c2088c7a36db…2026-10-15 13:18:30 2026-09 N212099-001 9657003 2030-10-27 U-4208 Drug substance, Drug product 2019-08-27 c2088c7a36db…2026-10-15 13:18:30 2026-09 N212099-001 9657003 2030-10-27 U-4210 Drug substance, Drug product 2019-08-27 c2088c7a36db…2026-10-15 13:18:30 2026-09 N212099-001 8975254 2033-03-25 U-4208 Drug substance, Drug product 2019-08-27 c2088c7a36db…2026-10-15 13:18:30 2026-09 N212099-001 8975254 2033-03-25 U-4210 Drug substance, Drug product 2019-08-27 c2088c7a36db…2026-10-15 13:18:30 2026-09 N212099-001 8975254 2033-03-25 U-4209 Drug substance, Drug product 2019-08-27 c2088c7a36db…2026-10-15 13:18:30 2026-09 N212099-001 10010530 2036-01-28 Drug substance 2019-08-27 c2088c7a36db…2026-10-15 13:18:30 2026-09 N212099-001 10383853 2036-01-28 Drug substance 2019-08-27 c2088c7a36db…2026-10-15 13:18:30 2026-09 N212099-001 10835515 2036-01-28 U-4210 Drug product 2020-12-11 c2088c7a36db…2026-10-15 13:18:30 2026-09 N212099-001 10835515 2036-01-28 U-4208 Drug product 2020-12-11 c2088c7a36db…2026-10-15 13:18:30 2026-09 N212099-001 10835515 2036-01-28 U-4209 Drug product 2020-12-11 c2088c7a36db…2026-10-15 13:18:30 2026-09 N212099-001 10835515 2036-01-28 U-2605 Drug product 2020-12-11 c2088c7a36db…2026-10-15 13:18:30 2026-09 N212099-001 11168058 2038-02-27 Drug substance, Drug product 2022-01-27 c2088c7a36db…2026-10-15 13:18:30 2026-09 N212099-001 12611397 2040-07-02 Drug product 2026-05-15 c2088c7a36db…2026-10-15 13:18:30 2026-09 N212099-001 12329742 2042-06-17 Drug product 2025-07-02 c2088c7a36db…2026-09-14 22:38:34 2026-08 N212099-001 10711013 2030-10-27 Drug substance, Drug product 2020-08-11 84e616aacf4f…2026-09-14 22:38:34 2026-08 N212099-001 11046713 2030-10-27 Drug substance 2021-07-28 84e616aacf4f…2026-09-14 22:38:34 2026-08 N212099-001 9657003 2030-10-27 U-4209 Drug substance, Drug product 2019-08-27 84e616aacf4f…2026-09-14 22:38:34 2026-08 N212099-001 9657003 2030-10-27 U-4208 Drug substance, Drug product 2019-08-27 84e616aacf4f…2026-09-14 22:38:34 2026-08 N212099-001 9657003 2030-10-27 U-4210 Drug substance, Drug product 2019-08-27 84e616aacf4f…2026-09-14 22:38:34 2026-08 N212099-001 8975254 2033-03-25 U-4208 Drug substance, Drug product 2019-08-27 84e616aacf4f…2026-09-14 22:38:34 2026-08 N212099-001 8975254 2033-03-25 U-4210 Drug substance, Drug product 2019-08-27 84e616aacf4f…2026-09-14 22:38:34 2026-08 N212099-001 8975254 2033-03-25 U-4209 Drug substance, Drug product 2019-08-27 84e616aacf4f…2026-09-14 22:38:34 2026-08 N212099-001 10010530 2036-01-28 Drug substance 2019-08-27 84e616aacf4f…2026-09-14 22:38:34 2026-08 N212099-001 10383853 2036-01-28 Drug substance 2019-08-27 84e616aacf4f…2026-09-14 22:38:34 2026-08 N212099-001 10835515 2036-01-28 U-4210 Drug product 2020-12-11 84e616aacf4f…2026-09-14 22:38:34 2026-08 N212099-001 10835515 2036-01-28 U-4208 Drug product 2020-12-11 84e616aacf4f…2026-09-14 22:38:34 2026-08 N212099-001 10835515 2036-01-28 U-4209 Drug product 2020-12-11 84e616aacf4f…2026-09-14 22:38:34 2026-08 N212099-001 10835515 2036-01-28 U-2605 Drug product 2020-12-11 84e616aacf4f…2026-09-14 22:38:34 2026-08 N212099-001 11168058 2038-02-27 Drug substance, Drug product 2022-01-27 84e616aacf4f…2026-09-14 22:38:34 2026-08 N212099-001 12611397 2040-07-02 Drug product 2026-05-15 84e616aacf4f…2026-09-14 22:38:34 2026-08 N212099-001 12329742 2042-06-17 Drug product 2025-07-02 84e616aacf4f…2026-08-18 06:07:40 2026-07 N212099-001 10711013 2030-10-27 Drug substance, Drug product 2020-08-11 caaa826d4ba7…2026-08-18 06:07:40 2026-07 N212099-001 11046713 2030-10-27 Drug substance 2021-07-28 caaa826d4ba7…2026-08-18 06:07:40 2026-07 N212099-001 9657003 2030-10-27 U-4209 Drug substance, Drug product 2019-08-27 caaa826d4ba7…2026-08-18 06:07:40 2026-07 N212099-001 9657003 2030-10-27 U-4208 Drug substance, Drug product 2019-08-27 caaa826d4ba7…2026-08-18 06:07:40 2026-07 N212099-001 9657003 2030-10-27 U-4210 Drug substance, Drug product 2019-08-27 caaa826d4ba7…2026-08-18 06:07:40 2026-07 N212099-001 8975254 2033-03-25 U-4208 Drug substance, Drug product 2019-08-27 caaa826d4ba7…
Observed Orange Book exclusivity history# Exclusivity history page 1 of 2 · 64 observed states.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
NDC Listings For This Application# NDC listings for this application page 1 of 1 · 8 matching rows.
NDC, Name, Nonproprietary name table NDC Name Nonproprietary name Labeler Marketing category Status 50419-395 NUBEQA darolutamide Bayer HealthCare Pharmaceuticals Inc. NDA Current 50419-395 NUBEQA darolutamide Bayer HealthCare Pharmaceuticals Inc. NDA Current 50419-395 NUBEQA darolutamide Bayer HealthCare Pharmaceuticals Inc. NDA Current 50419-395 NUBEQA darolutamide Bayer HealthCare Pharmaceuticals Inc. NDA Current 50419-395 NUBEQA darolutamide Bayer HealthCare Pharmaceuticals Inc. NDA Current 50419-395 NUBEQA darolutamide Bayer HealthCare Pharmaceuticals Inc. NDA Current 50419-395 NUBEQA darolutamide Bayer HealthCare Pharmaceuticals Inc. NDA Current 50419-395 NUBEQA darolutamide Bayer HealthCare Pharmaceuticals Inc. NDA Current
Documents# Document, Submission type, Date table Document Submission type Date 82460 SUPPL 2025-06-05 82466 SUPPL 2025-06-04 75780 SUPPL 2023-10-16 75732 SUPPL 2023-10-16 71775 SUPPL 2022-08-11 71739 SUPPL 2022-08-08 65873 SUPPL 2021-01-08 65871 SUPPL 2021-01-08 59870 ORIG 2019-08-29 59521 ORIG 2019-07-31 59518 ORIG 2019-07-31