Product NDC: | 67296-0543 |
Proprietary Name: | CIPROFLOXACIN HYDROCHLORIDE |
Non Proprietary Name: | ciprofloxacin hydrochloride tablet |
Active Ingredient(s): | 500 mg/1 & nbsp; ciprofloxacin hydrochloride tablet |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 67296-0543 |
Labeler Name: | RedPharm Drug Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA076089 |
Marketing Category: | ANDA |
Start Marketing Date: | 20110404 |
Package NDC: | 67296-0543-4 |
Package Description: | 6 TABLET in 1 BOTTLE (67296-0543-4) |
NDC Code | 67296-0543-4 |
Proprietary Name | CIPROFLOXACIN HYDROCHLORIDE |
Package Description | 6 TABLET in 1 BOTTLE (67296-0543-4) |
Product NDC | 67296-0543 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | ciprofloxacin hydrochloride tablet |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20110404 |
Marketing Category Name | ANDA |
Labeler Name | RedPharm Drug Inc. |
Substance Name | CIPROFLOXACIN HYDROCHLORIDE |
Strength Number | 500 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Quinolone Antimicrobial [EPC],Quinolones [Chemical/Ingredient] |