Ciprofloxacin - Ciprofloxacin
Navigation: NDC > Supplier starting with: A > AUROLIFE PHARMA LLC| Field | Value |
|---|---|
| NDC Code: | 13107-076 |
| Proprietary Name: | Ciprofloxacin |
| Suffix: | |
| Non-Proprietary Name: | Ciprofloxacin |
| Dosage Form: | TABLET, FILM COATED |
| Method: | ORAL |
| Original Marketing Date: | 01-08-2009 |
| Category Name: | ANDA |
| Application Number: | ANDA077859 |
| Labeler: | AUROLIFE PHARMA LLC |
| Substance Name: | CIPROFLOXACIN HYDROCHLORIDE |
| Active Numerator Strength: | 250 |
| Active Ingredient Unit: | mg/1 |
| Pharm Classes: | Quinolone Antimicrobial [EPC],Quinolones [Chemical/Ingredient] |
| DEA Schedule: |