Cipro - ciprofloxacin hydrochloride
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Field |
Value |
NDC Code: |
50419-758 |
Proprietary Name: |
Cipro |
Suffix: |
|
Non-Proprietary Name: |
ciprofloxacin hydrochloride |
Dosage Form: |
TABLET, FILM COATED |
Method: |
ORAL |
Original Marketing Date: |
22-10-1987 |
Category Name: |
NDA |
Application Number: |
NDA019537 |
Labeler: |
BAYER HEALTHCARE PHARMACEUTICALS INC. |
Substance Name: |
CIPROFLOXACIN HYDROCHLORIDE |
Active Numerator Strength: |
250 |
Active Ingredient Unit: |
mg/1 |
Pharm Classes: |
Quinolone Antimicrobial [EPC],Quinolones [Chemical/Ingredient] |
DEA Schedule: |
|