Home Applications 211109 Application 211109
Type NDA
Sponsor TETRAPHASE PHARMS Application Products# Product, Drug, Ingredient table Product Drug Ingredient Form Strength Reference drug Reference standard 001 XERAVA ERAVACYCLINE DIHYDROCHLORIDE POWDER;INTRAVENOUS EQ 50MG BASE/VIAL Yes Yes 002 XERAVA ERAVACYCLINE DIHYDROCHLORIDE POWDER;INTRAVENOUS EQ 100MG BASE/VIAL Yes No
Source provenance: Browse the complete Orange Book source catalog · source snapshot 44 .
Orange Book products# Current product rows page 1 of 1 · 2 matching rows.
Application-product, Trade name, Ingredient table Application-product Trade name Ingredient Strength Dosage form / route TE codes RLD / RS Approval date N211109-001 XERAVA ERAVACYCLINE DIHYDROCHLORIDE EQ 50MG BASE/VIAL POWDER / INTRAVENOUS RLD, RS 2018-08-27 N211109-002 XERAVA ERAVACYCLINE DIHYDROCHLORIDE EQ 100MG BASE/VIAL POWDER / INTRAVENOUS RLD, RS 2020-06-03
Orange Book patents# Current patent rows page 1 of 1 · 8 matching rows.
Application-product, Patent, Expiration table Application-product Patent Expiration Use code Coverage / status Submission date N211109-001 8796245 2029-08-07 U-2380 2018-09-13 N211109-001 8906887 2032-08-27 Drug product 2018-09-13 N211109-001 10961190 2037-10-19 Drug substance 2022-01-13 N211109-001 11578044 2037-10-19 Drug substance 2023-03-17 N211109-002 8796245 2029-08-07 U-2380 2021-12-15 N211109-002 8906887 2032-08-27 Drug product 2021-12-15 N211109-002 10961190 2037-10-19 Drug substance 2022-01-13 N211109-002 11578044 2037-10-19 Drug substance 2023-03-17
Orange Book exclusivity# Current exclusivity rows page 1 of 1 · 4 matching rows.
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 1 of 3 · 84 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 2026-10-15 13:18:30 2026-09 N211109-001 XERAVA EQ 50MG BASE/VIAL POWDER / INTRAVENOUS RLD, RS 2018-08-27 c2088c7a36db…2026-10-15 13:18:30 2026-09 N211109-002 XERAVA EQ 100MG BASE/VIAL POWDER / INTRAVENOUS RLD, RS 2020-06-03 c2088c7a36db…2026-09-14 22:38:34 2026-08 N211109-001 XERAVA EQ 50MG BASE/VIAL POWDER / INTRAVENOUS RLD, RS 2018-08-27 84e616aacf4f…2026-09-14 22:38:34 2026-08 N211109-002 XERAVA EQ 100MG BASE/VIAL POWDER / INTRAVENOUS RLD, RS 2020-06-03 84e616aacf4f…2026-08-18 06:07:40 2026-07 N211109-001 XERAVA EQ 50MG BASE/VIAL POWDER / INTRAVENOUS RLD, RS 2018-08-27 caaa826d4ba7…2026-08-18 06:07:40 2026-07 N211109-002 XERAVA EQ 100MG BASE/VIAL POWDER / INTRAVENOUS RLD, RS 2020-06-03 caaa826d4ba7…2026-02-19 14:30 UTC 2026-02 N211109-001 XERAVA EQ 50MG BASE/VIAL POWDER / INTRAVENOUS RLD, RS 2018-08-27 011fe1cb6892…2026-02-19 14:30 UTC 2026-02 N211109-002 XERAVA EQ 100MG BASE/VIAL POWDER / INTRAVENOUS RLD, RS 2020-06-03 011fe1cb6892…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 N211109-001 XERAVA EQ 50MG BASE/VIAL POWDER / INTRAVENOUS RLD, RS 2018-08-27 31067a03dcf5…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 N211109-002 XERAVA EQ 100MG BASE/VIAL POWDER / INTRAVENOUS RLD, RS 2020-06-03 31067a03dcf5…2025-08-23 18:47 UTC 2025-08 N211109-001 XERAVA EQ 50MG BASE/VIAL POWDER / INTRAVENOUS RLD, RS 2018-08-27 6a471c1ec25d…2025-08-23 18:47 UTC 2025-08 N211109-002 XERAVA EQ 100MG BASE/VIAL POWDER / INTRAVENOUS RLD, RS 2020-06-03 6a471c1ec25d…2025-03-22 03:13 UTC · 3 captures of this ZIP 2025-03 N211109-001 XERAVA EQ 50MG BASE/VIAL POWDER / INTRAVENOUS RLD, RS 2018-08-27 fd3edfee7708…2025-03-22 03:13 UTC · 3 captures of this ZIP 2025-03 N211109-002 XERAVA EQ 100MG BASE/VIAL POWDER / INTRAVENOUS RLD, RS 2020-06-03 fd3edfee7708…2025-02-26 10:13 UTC · 3 captures of this ZIP 2025-02 N211109-001 XERAVA EQ 50MG BASE/VIAL POWDER / INTRAVENOUS RLD, RS 2018-08-27 b8a1b40f171c…2025-02-26 10:13 UTC · 3 captures of this ZIP 2025-02 N211109-002 XERAVA EQ 100MG BASE/VIAL POWDER / INTRAVENOUS RLD, RS 2020-06-03 b8a1b40f171c…2025-01-19 17:59 UTC · 7 captures of this ZIP 2025-01 N211109-001 XERAVA EQ 50MG BASE/VIAL POWDER / INTRAVENOUS RLD, RS 2018-08-27 03ed91905a0d…2025-01-19 17:59 UTC · 7 captures of this ZIP 2025-01 N211109-002 XERAVA EQ 100MG BASE/VIAL POWDER / INTRAVENOUS RLD, RS 2020-06-03 03ed91905a0d…2024-12-13 21:23 UTC · 2 captures of this ZIP 2024-12 N211109-001 XERAVA EQ 50MG BASE/VIAL POWDER / INTRAVENOUS RLD, RS 2018-08-27 2680178bc6a6…2024-12-13 21:23 UTC · 2 captures of this ZIP 2024-12 N211109-002 XERAVA EQ 100MG BASE/VIAL POWDER / INTRAVENOUS RLD, RS 2020-06-03 2680178bc6a6…2024-09-14 05:58 UTC · 2 captures of this ZIP 2024-09 N211109-001 XERAVA EQ 50MG BASE/VIAL POWDER / INTRAVENOUS RLD, RS 2018-08-27 5bbf6a4d5a75…2024-09-14 05:58 UTC · 2 captures of this ZIP 2024-09 N211109-002 XERAVA EQ 100MG BASE/VIAL POWDER / INTRAVENOUS RLD, RS 2020-06-03 5bbf6a4d5a75…2024-11-08 22:44 UTC · 3 captures of this ZIP 2024-11 N211109-001 XERAVA EQ 50MG BASE/VIAL POWDER / INTRAVENOUS RLD, RS 2018-08-27 d8e5a09893c0…2024-11-08 22:44 UTC · 3 captures of this ZIP 2024-11 N211109-002 XERAVA EQ 100MG BASE/VIAL POWDER / INTRAVENOUS RLD, RS 2020-06-03 d8e5a09893c0…2024-10-29 15:01 UTC 2024-10 N211109-001 XERAVA EQ 50MG BASE/VIAL POWDER / INTRAVENOUS RLD, RS 2018-08-27 d06236e962d9…2024-10-29 15:01 UTC 2024-10 N211109-002 XERAVA EQ 100MG BASE/VIAL POWDER / INTRAVENOUS RLD, RS 2020-06-03 d06236e962d9…2024-08-13 05:28 UTC · 3 captures of this ZIP 2024-08 N211109-001 XERAVA EQ 50MG BASE/VIAL POWDER / INTRAVENOUS RLD, RS 2018-08-27 79d66fd596c7…2024-08-13 05:28 UTC · 3 captures of this ZIP 2024-08 N211109-002 XERAVA EQ 100MG BASE/VIAL POWDER / INTRAVENOUS RLD, RS 2020-06-03 79d66fd596c7…2024-07-13 05:37 UTC · 2 captures of this ZIP 2024-07 N211109-001 XERAVA EQ 50MG BASE/VIAL POWDER / INTRAVENOUS RLD, RS 2018-08-27 301d65b070ca…2024-07-13 05:37 UTC · 2 captures of this ZIP 2024-07 N211109-002 XERAVA EQ 100MG BASE/VIAL POWDER / INTRAVENOUS RLD, RS 2020-06-03 301d65b070ca…2024-06-18 03:08 UTC · 5 captures of this ZIP 2024-06 N211109-001 XERAVA EQ 50MG BASE/VIAL POWDER / INTRAVENOUS RLD, RS 2018-08-27 1e350fbaab3a…2024-06-18 03:08 UTC · 5 captures of this ZIP 2024-06 N211109-002 XERAVA EQ 100MG BASE/VIAL POWDER / INTRAVENOUS RLD, RS 2020-06-03 1e350fbaab3a…2024-05-31 18:47 UTC 2024-05 N211109-001 XERAVA EQ 50MG BASE/VIAL POWDER / INTRAVENOUS RLD, RS 2018-08-27 8072bd15b7f6…2024-05-31 18:47 UTC 2024-05 N211109-002 XERAVA EQ 100MG BASE/VIAL POWDER / INTRAVENOUS RLD, RS 2020-06-03 8072bd15b7f6…2022-06-29 02:47 UTC · 2 captures of this ZIP 2022-06 N211109-001 XERAVA EQ 50MG BASE/VIAL POWDER / INTRAVENOUS RLD, RS 2018-08-27 5c6f7cd8ea54…2022-06-29 02:47 UTC · 2 captures of this ZIP 2022-06 N211109-002 XERAVA EQ 100MG BASE/VIAL POWDER / INTRAVENOUS RLD, RS 2020-06-03 5c6f7cd8ea54…2022-04-08 23:34 UTC 2022-04 N211109-001 XERAVA EQ 50MG BASE/VIAL POWDER / INTRAVENOUS RLD, RS 2018-08-27 5d02ea3f76ae…2022-04-08 23:34 UTC 2022-04 N211109-002 XERAVA EQ 100MG BASE/VIAL POWDER / INTRAVENOUS RLD, RS 2020-06-03 5d02ea3f76ae…2022-04-04 05:41 UTC 2022-04 N211109-001 XERAVA EQ 50MG BASE/VIAL POWDER / INTRAVENOUS RLD, RS 2018-08-27 4b0b4de00fa7…2022-04-04 05:41 UTC 2022-04 N211109-002 XERAVA EQ 100MG BASE/VIAL POWDER / INTRAVENOUS RLD, RS 2020-06-03 4b0b4de00fa7…
Observed Orange Book patent history# Patent history page 1 of 7 · 280 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 N211109-001 8796245 2029-08-07 U-2380 2018-09-13 c2088c7a36db…2026-10-15 13:18:30 2026-09 N211109-001 8906887 2032-08-27 Drug product 2018-09-13 c2088c7a36db…2026-10-15 13:18:30 2026-09 N211109-001 10961190 2037-10-19 Drug substance 2022-01-13 c2088c7a36db…2026-10-15 13:18:30 2026-09 N211109-001 11578044 2037-10-19 Drug substance 2023-03-17 c2088c7a36db…2026-10-15 13:18:30 2026-09 N211109-002 8796245 2029-08-07 U-2380 2021-12-15 c2088c7a36db…2026-10-15 13:18:30 2026-09 N211109-002 8906887 2032-08-27 Drug product 2021-12-15 c2088c7a36db…2026-10-15 13:18:30 2026-09 N211109-002 10961190 2037-10-19 Drug substance 2022-01-13 c2088c7a36db…2026-10-15 13:18:30 2026-09 N211109-002 11578044 2037-10-19 Drug substance 2023-03-17 c2088c7a36db…2026-09-14 22:38:34 2026-08 N211109-001 8796245 2029-08-07 U-2380 2018-09-13 84e616aacf4f…2026-09-14 22:38:34 2026-08 N211109-001 8906887 2032-08-27 Drug product 2018-09-13 84e616aacf4f…2026-09-14 22:38:34 2026-08 N211109-001 10961190 2037-10-19 Drug substance 2022-01-13 84e616aacf4f…2026-09-14 22:38:34 2026-08 N211109-001 11578044 2037-10-19 Drug substance 2023-03-17 84e616aacf4f…2026-09-14 22:38:34 2026-08 N211109-002 8796245 2029-08-07 U-2380 2021-12-15 84e616aacf4f…2026-09-14 22:38:34 2026-08 N211109-002 8906887 2032-08-27 Drug product 2021-12-15 84e616aacf4f…2026-09-14 22:38:34 2026-08 N211109-002 10961190 2037-10-19 Drug substance 2022-01-13 84e616aacf4f…2026-09-14 22:38:34 2026-08 N211109-002 11578044 2037-10-19 Drug substance 2023-03-17 84e616aacf4f…2026-08-18 06:07:40 2026-07 N211109-001 8796245 2029-08-07 U-2380 2018-09-13 caaa826d4ba7…2026-08-18 06:07:40 2026-07 N211109-001 8906887 2032-08-27 Drug product 2018-09-13 caaa826d4ba7…2026-08-18 06:07:40 2026-07 N211109-001 10961190 2037-10-19 Drug substance 2022-01-13 caaa826d4ba7…2026-08-18 06:07:40 2026-07 N211109-001 11578044 2037-10-19 Drug substance 2023-03-17 caaa826d4ba7…2026-08-18 06:07:40 2026-07 N211109-002 8796245 2029-08-07 U-2380 2021-12-15 caaa826d4ba7…2026-08-18 06:07:40 2026-07 N211109-002 8906887 2032-08-27 Drug product 2021-12-15 caaa826d4ba7…2026-08-18 06:07:40 2026-07 N211109-002 10961190 2037-10-19 Drug substance 2022-01-13 caaa826d4ba7…2026-08-18 06:07:40 2026-07 N211109-002 11578044 2037-10-19 Drug substance 2023-03-17 caaa826d4ba7…2026-02-19 14:30 UTC 2026-02 N211109-001 8796245 2029-08-07 U-2380 2018-09-13 011fe1cb6892…2026-02-19 14:30 UTC 2026-02 N211109-001 8906887 2030-12-28 Drug product 2018-09-13 011fe1cb6892…2026-02-19 14:30 UTC 2026-02 N211109-001 10961190 2037-10-19 Drug substance 2022-01-13 011fe1cb6892…2026-02-19 14:30 UTC 2026-02 N211109-001 11578044 2037-10-19 Drug substance 2023-03-17 011fe1cb6892…2026-02-19 14:30 UTC 2026-02 N211109-002 8796245 2029-08-07 U-2380 2021-12-15 011fe1cb6892…2026-02-19 14:30 UTC 2026-02 N211109-002 8906887 2030-12-28 Drug product 2021-12-15 011fe1cb6892…2026-02-19 14:30 UTC 2026-02 N211109-002 10961190 2037-10-19 Drug substance 2022-01-13 011fe1cb6892…2026-02-19 14:30 UTC 2026-02 N211109-002 11578044 2037-10-19 Drug substance 2023-03-17 011fe1cb6892…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 N211109-001 8796245 2029-08-07 U-2380 2018-09-13 31067a03dcf5…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 N211109-001 8906887 2030-12-28 Drug product 2018-09-13 31067a03dcf5…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 N211109-001 10961190 2037-10-19 Drug substance 2022-01-13 31067a03dcf5…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 N211109-001 11578044 2037-10-19 Drug substance 2023-03-17 31067a03dcf5…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 N211109-002 8796245 2029-08-07 U-2380 2021-12-15 31067a03dcf5…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 N211109-002 8906887 2030-12-28 Drug product 2021-12-15 31067a03dcf5…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 N211109-002 10961190 2037-10-19 Drug substance 2022-01-13 31067a03dcf5…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 N211109-002 11578044 2037-10-19 Drug substance 2023-03-17 31067a03dcf5…
Observed Orange Book exclusivity history# Exclusivity history page 1 of 4 · 160 observed states.
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 1 of 1 · 1 matching rows.
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 · 7 matching rows.
NDC, Name, Nonproprietary name table NDC Name Nonproprietary name Labeler Marketing category Status 71773-050 Xerava eravacycline Tetraphase Pharmaceuticals, Inc. NDA Current 71773-050 Xerava eravacycline Tetraphase Pharmaceuticals, Inc. NDA Current 71773-050 Xerava eravacycline Tetraphase Pharmaceuticals, Inc. NDA Current 71773-050 Xerava eravacycline Tetraphase Pharmaceuticals, Inc. NDA Current 71773-050 Xerava eravacycline Tetraphase Pharmaceuticals, Inc. NDA Current 71773-100 Xerava eravacycline Tetraphase Pharmaceuticals, Inc. NDA Current 71773-100 Xerava eravacycline Tetraphase Pharmaceuticals, Inc. NDA Current
Documents# Document, Submission type, Date table Document Submission type Date 81864 SUPPL 2025-04-08 81798 SUPPL 2025-04-02 80590 SUPPL 2024-12-16 80577 SUPPL 2024-12-16 63656 SUPPL 2020-06-22 55782 ORIG 2018-10-02 55343 ORIG 2018-08-28 55342 ORIG 2018-08-28