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ciprofloxacin hydrochloride
ciprofloxacin hydrochloride - 53401-005-20 - (ciprofloxacin hydrochloride)
Drug Information of ciprofloxacin hydrochloride
| Product NDC: | 53401-005 |
| Proprietary Name: | ciprofloxacin hydrochloride |
| Non Proprietary Name: | ciprofloxacin hydrochloride |
| Active Ingredient(s): | 500 mg/1 & nbsp; ciprofloxacin hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of ciprofloxacin hydrochloride
| Product NDC: | 53401-005 |
| Labeler Name: | Testpak Holding Company |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA076794 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20091203 |
Package Information of ciprofloxacin hydrochloride
| Package NDC: | 53401-005-20 |
| Package Description: | 20 TABLET, COATED in 1 BOTTLE (53401-005-20) |
NDC Information of ciprofloxacin hydrochloride
| NDC Code | 53401-005-20 |
| Proprietary Name | ciprofloxacin hydrochloride |
| Package Description | 20 TABLET, COATED in 1 BOTTLE (53401-005-20) |
| Product NDC | 53401-005 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | ciprofloxacin hydrochloride |
| Dosage Form Name | TABLET, COATED |
| Route Name | ORAL |
| Start Marketing Date | 20091203 |
| Marketing Category Name | ANDA |
| Labeler Name | Testpak Holding Company |
| Substance Name | CIPROFLOXACIN HYDROCHLORIDE |
| Strength Number | 500 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Quinolone Antimicrobial [EPC],Quinolones [Chemical/Ingredient] |
