Product NDC: | 68788-9724 |
Proprietary Name: | Ciprofloxacin |
Non Proprietary Name: | Ciprofloxacin Hydrochloride |
Active Ingredient(s): | 250 mg/1 & nbsp; Ciprofloxacin Hydrochloride |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, FILM COATED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 68788-9724 |
Labeler Name: | Preferred Pharmaceuticals, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA077859 |
Marketing Category: | ANDA |
Start Marketing Date: | 20121121 |
Package NDC: | 68788-9724-0 |
Package Description: | 6 TABLET, FILM COATED in 1 BOTTLE (68788-9724-0) |
NDC Code | 68788-9724-0 |
Proprietary Name | Ciprofloxacin |
Package Description | 6 TABLET, FILM COATED in 1 BOTTLE (68788-9724-0) |
Product NDC | 68788-9724 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Ciprofloxacin Hydrochloride |
Dosage Form Name | TABLET, FILM COATED |
Route Name | ORAL |
Start Marketing Date | 20121121 |
Marketing Category Name | ANDA |
Labeler Name | Preferred Pharmaceuticals, Inc. |
Substance Name | CIPROFLOXACIN HYDROCHLORIDE |
Strength Number | 250 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Quinolone Antimicrobial [EPC],Quinolones [Chemical/Ingredient] |