Overview
No overview information available.
Indication
No indication information available.
Associated Conditions
No associated conditions information available.
Clinical Trials
Title | Posted | Study ID | Phase | Status | Sponsor |
|---|
No clinical trials found
No clinical trials found for this drug
FDA Drug Approvals
Approved Product | Manufacturer | NDC Code | Route | Strength | Effective Date |
|---|---|---|---|---|---|
| Imprimis NJOF, LLC | 71384-513 | OPHTHALMIC | 0.5 mg in 1 mL | 2/10/2020 | |
| DIRECT RX | 61919-553 | OPHTHALMIC | 5 mg in 1 mL | 7/30/2018 | |
| Imprimis NJOF, LLC | 71384-512 | OPHTHALMIC | 5 mg in 1 mL | 2/10/2020 | |
| Imprimis NJOF, LLC | 71384-510 | OPHTHALMIC | 1 mg in 1 mL | 2/10/2020 | |
| Direct Rx | 72189-321 | OPHTHALMIC | 5 mg in 1 mL | 2/7/2022 | |
| Apotex Corp. | 60505-0582 | OPHTHALMIC | 5 mg in 1 mL | 9/19/2025 | |
| Redpharm Drug | 67296-2129 | OPHTHALMIC | 5 mg in 1 mL | 6/10/2025 | |
| Bryant Ranch Prepack | 72162-2107 | OPHTHALMIC | 5 mg in 1 mL | 9/19/2023 | |
| Advanced Rx Pharmacy of Tennessee, LLC | 80425-0379 | OPHTHALMIC | 5 mg in 1 mL | 3/21/2024 | |
| ImprimisRx NJ | 70261-513 | INTRAOCULAR | 0.5 mg in 1 mL | 5/8/2018 |
EMA Drug Approvals
Approved Product | Authorization Holder | Status | Issued Date |
|---|---|---|---|
| No EMA approvals found for this drug. | |||
HSA Drug Approvals
Approved Product | Manufacturer | Approval Number | Dosage Form | Strength | Approval Date |
|---|---|---|---|---|---|
| No HSA approvals found for this drug. | |||||
NMPA Drug Approvals
Approved Product | Company | Approval Number | Drug Type | Dosage Form | Approval Date |
|---|---|---|---|---|---|
| No NMPA approvals found for this drug. | |||||
PPB Drug Approvals
Approved Product | Registration No. | Company | Licence No. | Strength | Registration Date |
|---|---|---|---|---|---|
| No PPB approvals found for this drug. | |||||
TGA Drug Approvals
Approved Product | ARTG ID | Sponsor | Registration Type | Status | Registration Date |
|---|---|---|---|---|---|
| MOXIFLOXACIN MEDICIANZ moxifloxacin (as hydrochloride monohydrate) 400 mg tablet blister pack | 398595 | Medicine | A | 12/20/2023 | |
| MOXIFLOXACIN MEDSURGE moxifloxacin (as hydrochloride monohydrate) 400 mg tablet blister pack | 398594 | Medicine | A | 12/20/2023 | |
| GenRx MOXIFLOXACIN moxifloxacin (as hydrochloride monohydrate) 400 mg film coated tablet blister pack | 223566 | Medicine | A | 3/15/2016 | |
| MOXIFLOXACIN APO moxifloxacin (as hydrochloride monohydrate) 400 mg tablet blister pack | 309824 | Medicine | A | 8/9/2019 | |
| MOXIFLOXACIN B&B moxifloxacin (as hydrochloride monohydrate) 400 mg tablet blister pack | 398593 | Medicine | A | 12/20/2023 | |
| MOXIFLOXACIN MLabs moxifloxacin (as hydrochloride monohydrate) 400 mg tablet blister pack | 398591 | Medicine | A | 12/20/2023 | |
| MOXIMED moxifloxacin (as hydrochloride monohydrate) 400 mg tablet blister pack | 398590 | Medicine | A | 12/20/2023 | |
| MOXEZIN moxifloxacin (as hydrochloride monohydrate) 400 mg tablet blister pack | 398592 | Medicine | A | 12/20/2023 |
Health Canada Drug Approvals
Approved Product | Company | DIN | Dosage Form | Strength | Market Date |
|---|---|---|---|---|---|
| No Health Canada approvals found for this drug. | |||||
CIMA AEMPS Drug Approvals
Approved Product | Company | Registration Number | Pharmaceutical Form | Prescription Type | Status |
|---|---|---|---|---|---|
| No CIMA AEMPS (Spain) approvals found for this drug. | |||||
Philippines FDA Drug Approvals
Approved Product | Company | License Number | Dosage Form | Strength | Approval Date |
|---|---|---|---|---|---|
| No Philippines FDA approvals found for this drug. | |||||
Saudi SFDA Drug Approvals
Approved Product | Company | License Number | Dosage Form | Strength | Approval Date |
|---|---|---|---|---|---|
| No Saudi SFDA approvals found for this drug. | |||||
Malaysia NPRA Drug Approvals
Approved Product | Company | Registration Number | Dosage Form | Strength | Approval Date |
|---|---|---|---|---|---|
| No Malaysia NPRA approvals found for this drug. | |||||
UK EMC Drug Information
Medicine Name | MA Holder | MA Number | Pharmaceutical Form | Active Ingredient | Authorization Date |
|---|---|---|---|---|---|
| No UK EMC drug information found for this drug. | |||||
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