ciprofloxacin hydrochloride - ciprofloxacin hydrochloride
Navigation: NDC > Supplier starting with: T > TESTPAK HOLDING COMPANY| Field | Value |
|---|---|
| NDC Code: | 53401-005 |
| Proprietary Name: | ciprofloxacin hydrochloride |
| Suffix: | |
| Non-Proprietary Name: | ciprofloxacin hydrochloride |
| Dosage Form: | TABLET, COATED |
| Method: | ORAL |
| Original Marketing Date: | 03-12-2009 |
| Category Name: | ANDA |
| Application Number: | ANDA076794 |
| Labeler: | TESTPAK HOLDING COMPANY |
| Substance Name: | CIPROFLOXACIN HYDROCHLORIDE |
| Active Numerator Strength: | 500 |
| Active Ingredient Unit: | mg/1 |
| Pharm Classes: | Quinolone Antimicrobial [EPC],Quinolones [Chemical/Ingredient] |
| DEA Schedule: |