Details for New Drug Application (NDA): 208682
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The generic ingredient in MOXIFLOXACIN HYDROCHLORIDE is moxifloxacin hydrochloride. There are eighteen drug master file entries for this compound. Thirty-five suppliers are listed for this compound. Additional details are available on the moxifloxacin hydrochloride profile page.
Summary for 208682
Tradename: | MOXIFLOXACIN HYDROCHLORIDE |
Applicant: | Msn |
Ingredient: | moxifloxacin hydrochloride |
Patents: | 0 |
Suppliers and Packaging for NDA: 208682
Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
---|---|---|---|---|---|---|---|---|
MOXIFLOXACIN HYDROCHLORIDE | moxifloxacin hydrochloride | TABLET;ORAL | 208682 | ANDA | MSN LABORATORIES PRIVATE LIMITED | 69539-006 | 69539-006-05 | 500 TABLET, FILM COATED in 1 BOTTLE (69539-006-05) |
MOXIFLOXACIN HYDROCHLORIDE | moxifloxacin hydrochloride | TABLET;ORAL | 208682 | ANDA | MSN LABORATORIES PRIVATE LIMITED | 69539-006 | 69539-006-30 | 30 TABLET, FILM COATED in 1 BOTTLE (69539-006-30) |
Profile for product number 001
Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | EQ 400MG BASE | ||||
Approval Date: | Sep 22, 2017 | TE: | AB | RLD: | No |
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