| NDC Code: |
62037-938 |
| Proprietary Name: |
Ciprofloxacin |
| Suffix: |
|
| Non-Proprietary Name: |
Ciprofloxacin |
| Dosage Form: |
TABLET, FILM COATED, EXTENDED RELEASE |
| Method: |
ORAL |
| Original Marketing Date: |
30-11-2010 |
| Category Name: |
ANDA |
| Application Number: |
ANDA077809 |
| Labeler: |
WATSON PHARMA, INC. |
| Substance Name: |
CIPROFLOXACIN; CIPROFLOXACIN HYDROCHLORIDE |
| Active Numerator Strength: |
425.2; 574.9 |
| Active Ingredient Unit: |
mg/1; mg/1 |
| Pharm Classes: |
Quinolone Antimicrobial [EPC],Quinolones [Chemical/Ingredient],Quinolone Antimicrobial [EPC],Quinolones [Chemical/Ingredient] |
| DEA Schedule: |
|
