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Ciprofloxacin
Ciprofloxacin - 21695-210-10 - (ciprofloxacin hydrochloride)
Drug Information of Ciprofloxacin
| Product NDC: | 21695-210 |
| Proprietary Name: | Ciprofloxacin |
| Non Proprietary Name: | ciprofloxacin hydrochloride |
| Active Ingredient(s): | 500 mg/1 & nbsp; ciprofloxacin hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Ciprofloxacin
| Product NDC: | 21695-210 |
| Labeler Name: | Rebel Distributors Corp. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA076794 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20040609 |
Package Information of Ciprofloxacin
| Package NDC: | 21695-210-10 |
| Package Description: | 10 TABLET, FILM COATED in 1 BOTTLE (21695-210-10) |
NDC Information of Ciprofloxacin
| NDC Code | 21695-210-10 |
| Proprietary Name | Ciprofloxacin |
| Package Description | 10 TABLET, FILM COATED in 1 BOTTLE (21695-210-10) |
| Product NDC | 21695-210 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | ciprofloxacin hydrochloride |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20040609 |
| Marketing Category Name | ANDA |
| Labeler Name | Rebel Distributors Corp. |
| Substance Name | CIPROFLOXACIN HYDROCHLORIDE |
| Strength Number | 500 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Quinolone Antimicrobial [EPC],Quinolones [Chemical/Ingredient] |
