Product NDC: | 63629-3868 |
Proprietary Name: | Ciprofloxacin |
Non Proprietary Name: | Ciprofloxacin |
Active Ingredient(s): | 750 mg/1 & nbsp; Ciprofloxacin |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, FILM COATED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 63629-3868 |
Labeler Name: | Bryant Ranch Prepack |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA076558 |
Marketing Category: | ANDA |
Start Marketing Date: | 20040609 |
Package NDC: | 63629-3868-7 |
Package Description: | 90 TABLET, FILM COATED in 1 BOTTLE (63629-3868-7) |
NDC Code | 63629-3868-7 |
Proprietary Name | Ciprofloxacin |
Package Description | 90 TABLET, FILM COATED in 1 BOTTLE (63629-3868-7) |
Product NDC | 63629-3868 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Ciprofloxacin |
Dosage Form Name | TABLET, FILM COATED |
Route Name | ORAL |
Start Marketing Date | 20040609 |
Marketing Category Name | ANDA |
Labeler Name | Bryant Ranch Prepack |
Substance Name | CIPROFLOXACIN |
Strength Number | 750 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Quinolone Antimicrobial [EPC],Quinolones [Chemical/Ingredient] |