Details for New Drug Application (NDA): 020013
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The generic ingredient in MAXAQUIN is lomefloxacin hydrochloride. There is one drug master file entry for this compound. Additional details are available on the lomefloxacin hydrochloride profile page.
Summary for 020013
| Tradename: | MAXAQUIN |
| Applicant: | Pharmacia |
| Ingredient: | lomefloxacin hydrochloride |
| Patents: | 0 |
Profile for product number 001
| Active Rx/OTC/Discontinued: | DISCN | Dosage: | TABLET;ORAL | Strength | EQ 400MG BASE | ||||
| Approval Date: | Feb 21, 1992 | TE: | RLD: | No | |||||
Expired US Patents for NDA 020013
| Applicant | Tradename | Generic Name | Dosage | NDA | Approval Date | Patent No. | Patent Expiration |
|---|---|---|---|---|---|---|---|
| Pharmacia | MAXAQUIN | lomefloxacin hydrochloride | TABLET;ORAL | 020013-001 | Feb 21, 1992 | ⤷ Start Trial | ⤷ Start Trial |
| >Applicant | >Tradename | >Generic Name | >Dosage | >NDA | >Approval Date | >Patent No. | >Patent Expiration |
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