Application 020394
- Type
- NDA
- Sponsor
- BOEHRINGER INGELHEIM
Application Products#
| Product | Drug | Ingredient | Form | Strength | Reference drug | Reference standard |
|---|---|---|---|---|---|---|
| 001 | ATROVENT | IPRATROPIUM BROMIDE | SPRAY, METERED;NASAL | 0.042MG/SPRAY | Yes | No |
Orange Book products#
| Application-product | Trade name | Ingredient | Strength | Dosage form / route | TE codes | RLD / RS | Approval date |
|---|---|---|---|---|---|---|---|
| N020394-001 | ATROVENT | IPRATROPIUM BROMIDE | 0.042MG/SPRAY **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | SPRAY, METERED / NASAL | RLD | 1995-10-20 |
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.
| Captured | Edition | Application-product | Trade name | Strength | Dosage form / route | Product TE source text | RLD / RS | Approval date | Source SHA-256 |
|---|---|---|---|---|---|---|---|---|---|
| 2026-09-14 22:38:34 | 2026-08 | N020394-001 | ATROVENT | 0.042MG/SPRAY **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | SPRAY, METERED / NASAL | RLD | 1995-10-20 | 84e616aacf4f… | |
| 2026-08-18 06:07:40 | 2026-07 | N020394-001 | ATROVENT | 0.042MG/SPRAY **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | SPRAY, METERED / NASAL | RLD | 1995-10-20 | caaa826d4ba7… | |
| 2026-02-19 14:30 UTC | 2026-02 | N020394-001 | ATROVENT | 0.042MG/SPRAY **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | SPRAY, METERED / NASAL | RLD | 1995-10-20 | 011fe1cb6892… | |
| 2025-12-14 10:44 UTC · 2 captures of this ZIP | 2025-12 | N020394-001 | ATROVENT | 0.042MG/SPRAY **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | SPRAY, METERED / NASAL | RLD | 1995-10-20 | 31067a03dcf5… | |
| 2025-08-23 18:47 UTC | 2025-08 | N020394-001 | ATROVENT | 0.042MG/SPRAY **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | SPRAY, METERED / NASAL | RLD | 1995-10-20 | 6a471c1ec25d… | |
| 2025-03-22 03:13 UTC · 3 captures of this ZIP | 2025-03 | N020394-001 | ATROVENT | 0.042MG/SPRAY **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | SPRAY, METERED / NASAL | RLD | 1995-10-20 | fd3edfee7708… | |
| 2025-02-26 10:13 UTC · 3 captures of this ZIP | 2025-02 | N020394-001 | ATROVENT | 0.042MG/SPRAY **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | SPRAY, METERED / NASAL | RLD | 1995-10-20 | b8a1b40f171c… | |
| 2025-01-19 17:59 UTC · 7 captures of this ZIP | 2025-01 | N020394-001 | ATROVENT | 0.042MG/SPRAY **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | SPRAY, METERED / NASAL | RLD | 1995-10-20 | 03ed91905a0d… | |
| 2024-12-13 21:23 UTC · 2 captures of this ZIP | 2024-12 | N020394-001 | ATROVENT | 0.042MG/SPRAY **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | SPRAY, METERED / NASAL | RLD | 1995-10-20 | 2680178bc6a6… | |
| 2024-09-14 05:58 UTC · 2 captures of this ZIP | 2024-09 | N020394-001 | ATROVENT | 0.042MG/SPRAY **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | SPRAY, METERED / NASAL | RLD | 1995-10-20 | 5bbf6a4d5a75… | |
| 2024-11-08 22:44 UTC · 3 captures of this ZIP | 2024-11 | N020394-001 | ATROVENT | 0.042MG/SPRAY **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | SPRAY, METERED / NASAL | RLD | 1995-10-20 | d8e5a09893c0… | |
| 2024-10-29 15:01 UTC | 2024-10 | N020394-001 | ATROVENT | 0.042MG/SPRAY **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | SPRAY, METERED / NASAL | RLD | 1995-10-20 | d06236e962d9… | |
| 2024-08-13 05:28 UTC · 3 captures of this ZIP | 2024-08 | N020394-001 | ATROVENT | 0.042MG/SPRAY **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | SPRAY, METERED / NASAL | RLD | 1995-10-20 | 79d66fd596c7… | |
| 2024-07-13 05:37 UTC · 2 captures of this ZIP | 2024-07 | N020394-001 | ATROVENT | 0.042MG/SPRAY **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | SPRAY, METERED / NASAL | RLD | 1995-10-20 | 301d65b070ca… | |
| 2024-06-18 03:08 UTC · 5 captures of this ZIP | 2024-06 | N020394-001 | ATROVENT | 0.042MG/SPRAY **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | SPRAY, METERED / NASAL | RLD | 1995-10-20 | 1e350fbaab3a… | |
| 2024-05-31 18:47 UTC | 2024-05 | N020394-001 | ATROVENT | 0.042MG/SPRAY **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | SPRAY, METERED / NASAL | RLD | 1995-10-20 | 8072bd15b7f6… | |
| 2022-06-29 02:47 UTC · 2 captures of this ZIP | 2022-06 | N020394-001 | ATROVENT | 0.042MG/SPRAY **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | SPRAY, METERED / NASAL | RLD | 1995-10-20 | 5c6f7cd8ea54… | |
| 2022-04-08 23:34 UTC | 2022-04 | N020394-001 | ATROVENT | 0.042MG/SPRAY | SPRAY, METERED / NASAL | RLD | 1995-10-20 | 5d02ea3f76ae… | |
| 2022-04-04 05:41 UTC | 2022-04 | N020394-001 | ATROVENT | 0.042MG/SPRAY | SPRAY, METERED / NASAL | RLD | 1995-10-20 | 4b0b4de00fa7… | |
| 2019-12-13 00:20 UTC | 2019-12 | N020394-001 | ATROVENT | 0.042MG/SPRAY | SPRAY, METERED / NASAL | RLD | 1995-10-20 | 74a2ff9319b5… | |
| 2022-03-09 01:35 UTC | 2022-03 | N020394-001 | ATROVENT | 0.042MG/SPRAY **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | SPRAY, METERED / NASAL | RLD | 1995-10-20 | bb7c543d1eb4… | |
| 2021-12-28 21:50 UTC | 2021-12 | N020394-001 | ATROVENT | 0.042MG/SPRAY **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons** | SPRAY, METERED / NASAL | RLD | 1995-10-20 | 782e0a99824c… | |
| 2021-05-05 16:15 UTC · 3 captures of this ZIP | 2021-05 | N020394-001 | ATROVENT | 0.042MG/SPRAY | SPRAY, METERED / NASAL | RLD | 1995-10-20 | 87673890dc5c… | |
| 2021-03-12 10:30 UTC | 2021-03 | N020394-001 | ATROVENT | 0.042MG/SPRAY | SPRAY, METERED / NASAL | RLD | 1995-10-20 | 5aa47cf7b7d7… | |
| 2020-12-22 03:56 UTC | 2020-12 | N020394-001 | ATROVENT | 0.042MG/SPRAY | SPRAY, METERED / NASAL | RLD | 1995-10-20 | 8869cabd3fbd… | |
| 2020-11-12 02:37 UTC | 2020-11 | N020394-001 | ATROVENT | 0.042MG/SPRAY | SPRAY, METERED / NASAL | RLD | 1995-10-20 | c0c555d07b60… | |
| 2019-12-14 00:12 UTC | 2019-12 | N020394-001 | ATROVENT | 0.042MG/SPRAY | SPRAY, METERED / NASAL | RLD | 1995-10-20 | 3f01610625f2… | |
| 2019-09-15 20:21 UTC | 2019-09 | N020394-001 | ATROVENT | 0.042MG/SPRAY | SPRAY, METERED / NASAL | RLD | 1995-10-20 | b00525d2431f… | |
| 2019-07-19 19:46 UTC | 2019-07 | N020394-001 | ATROVENT | 0.042MG/SPRAY | SPRAY, METERED / NASAL | RLD | 1995-10-20 | ea99ee380514… | |
| 2024-03-16 18:09 UTC · 4 captures of this ZIP | 2024-03 | N020394-001 | ATROVENT | 0.042MG/SPRAY **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | SPRAY, METERED / NASAL | RLD | 1995-10-20 | 6a51e52b5d6a… | |
| 2024-02-18 07:12 UTC | 2024-02 | N020394-001 | ATROVENT | 0.042MG/SPRAY **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | SPRAY, METERED / NASAL | RLD | 1995-10-20 | 1c564ffb4f44… | |
| 2023-12-20 04:57 UTC | 2023-12 | N020394-001 | ATROVENT | 0.042MG/SPRAY **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | SPRAY, METERED / NASAL | RLD | 1995-10-20 | ea1830bbd6c7… | |
| 2023-11-28 05:40 UTC · 2 captures of this ZIP | 2023-11 | N020394-001 | ATROVENT | 0.042MG/SPRAY **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | SPRAY, METERED / NASAL | RLD | 1995-10-20 | a72a2bbeb626… | |
| 2023-10-25 00:34 UTC · 2 captures of this ZIP | 2023-10 | N020394-001 | ATROVENT | 0.042MG/SPRAY **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | SPRAY, METERED / NASAL | RLD | 1995-10-20 | 9b2671bbb829… | |
| 2023-07-15 15:27 UTC · 2 captures of this ZIP | 2023-07 | N020394-001 | ATROVENT | 0.042MG/SPRAY **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | SPRAY, METERED / NASAL | RLD | 1995-10-20 | a67488948f0b… | |
| 2023-06-13 01:57 UTC · 3 captures of this ZIP | 2023-06 | N020394-001 | ATROVENT | 0.042MG/SPRAY **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | SPRAY, METERED / NASAL | RLD | 1995-10-20 | 3f0d92c62455… | |
| 2023-05-13 08:27 UTC | 2023-05 | N020394-001 | ATROVENT | 0.042MG/SPRAY **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | SPRAY, METERED / NASAL | RLD | 1995-10-20 | 053a50430f4f… | |
| 2023-01-26 05:58 UTC | 2023-01 | N020394-001 | ATROVENT | 0.042MG/SPRAY **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | SPRAY, METERED / NASAL | RLD | 1995-10-20 | 3bdfa0b2c4d7… | |
| 2022-11-12 20:34 UTC · 5 captures of this ZIP | 2022-11 | N020394-001 | ATROVENT | 0.042MG/SPRAY **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | SPRAY, METERED / NASAL | RLD | 1995-10-20 | 3a93d1ddd44b… | |
| 2022-10-28 04:53 UTC | 2022-10 | N020394-001 | ATROVENT | 0.042MG/SPRAY **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | SPRAY, METERED / NASAL | RLD | 1995-10-20 | f41ea6bd6efb… |
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Ipratropium Bromide | IPRATROPIUM BROMIDE | American Health Packaging | 8927f392-4c88-4ac1-a934-c444ecf6b2c8 | 2024-06-03 | Warnings, Adverse reactions | IPRATROPIUM BROMIDE |
| Ipratropium Bromide | IPRATROPIUM BROMIDE | Amneal Pharmaceuticals NY LLC | 61820346-29d9-4864-b8f4-4a198b8ac594 | 2023-12-30 | Warnings, Adverse reactions | IPRATROPIUM BROMIDE |
| Ipratropium Bromide | IPRATROPIUM BROMIDE | Amneal Pharmaceuticals NY LLC | 3bda47b0-0326-49de-83f5-03b9ec6461f1 | 2023-12-30 | Warnings, Adverse reactions | IPRATROPIUM BROMIDE |
| Ipratropium Bromide | IPRATROPIUM BROMIDE | Bryant Ranch Prepack | fcf20db7-091d-40de-8755-03773fc47edd | 2023-12-07 | IPRATROPIUM BROMIDE | |
| Ipratropium bromide | IPRATROPIUM BROMIDE | Aurobindo Pharma Limited | ff2b6bda-4acd-41fd-8970-458c5265df21 | 2023-10-30 | Warnings, Adverse reactions | IPRATROPIUM BROMIDE |
| Ipratropium Bromide | IPRATROPIUM BROMIDE | A-S Medication Solutions | 9f7b2f09-e831-4e15-b226-5cef3b613bd1 | 2023-02-16 | Warnings, Adverse reactions | IPRATROPIUM BROMIDE |
| Ipratropium Bromide | IPRATROPIUM BROMIDE | Hikma Pharmaceuticals USA Inc. | 71bdbbb9-8696-416d-bed4-7259929c0161 | 2022-07-01 | Warnings, Adverse reactions | IPRATROPIUM BROMIDE |
| Ipratropium Bromide | IPRATROPIUM BROMIDE | Hikma Pharmaceuticals USA Inc. | 05c56190-e346-4674-a4f8-049ce632ce2d | 2022-07-01 | IPRATROPIUM BROMIDE | |
| Ipratropium Bromide | IPRATROPIUM BROMIDE | Sun Pharmaceutical Industries, Inc. | 231ae8f2-1ec9-4e0f-90a8-11d7b6222576 | 2022-04-13 | Warnings, Adverse reactions | IPRATROPIUM BROMIDE |
| Ipratropium Bromide | IPRATROPIUM BROMIDE | Bausch & Lomb Incorporated | 3fd850a2-af0f-4291-af5d-52c8d6094e64 | 2019-05-01 | Warnings, Adverse reactions | IPRATROPIUM BROMIDE |
| Ipratropium bromide | IPRATROPIUM BROMIDE | Bausch & Lomb Incorporated | 1e92b86d-66e1-45e4-9e23-f9310c95bf82 | 2019-05-01 | Warnings, Adverse reactions | IPRATROPIUM BROMIDE |
| Ipratropium Bromide | IPRATROPIUM BROMIDE | Mylan Pharmaceuticals Inc. | f625d3e3-c175-4d9a-99ea-dab410b262f1 | 2013-06-24 | Warnings, Adverse reactions | IPRATROPIUM BROMIDE |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.