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Ciprofloxacin Hydrochloride
Ciprofloxacin Hydrochloride - 0172-5313-10 - (Ciprofloxacin Hydrochloride)
Drug Information of Ciprofloxacin Hydrochloride
| Product NDC: | 0172-5313 |
| Proprietary Name: | Ciprofloxacin Hydrochloride |
| Non Proprietary Name: | Ciprofloxacin Hydrochloride |
| Active Ingredient(s): | 750 mg/1 & nbsp; Ciprofloxacin Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Ciprofloxacin Hydrochloride
| Product NDC: | 0172-5313 |
| Labeler Name: | Ivax Pharmaceuticals Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA076089 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20040609 |
Package Information of Ciprofloxacin Hydrochloride
| Package NDC: | 0172-5313-10 |
| Package Description: | 100 BLISTER PACK in 1 BOX, UNIT-DOSE (0172-5313-10) > 1 TABLET in 1 BLISTER PACK (0172-5313-00) |
NDC Information of Ciprofloxacin Hydrochloride
| NDC Code | 0172-5313-10 |
| Proprietary Name | Ciprofloxacin Hydrochloride |
| Package Description | 100 BLISTER PACK in 1 BOX, UNIT-DOSE (0172-5313-10) > 1 TABLET in 1 BLISTER PACK (0172-5313-00) |
| Product NDC | 0172-5313 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Ciprofloxacin Hydrochloride |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20040609 |
| Marketing Category Name | ANDA |
| Labeler Name | Ivax Pharmaceuticals Inc. |
| Substance Name | CIPROFLOXACIN HYDROCHLORIDE |
| Strength Number | 750 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Quinolone Antimicrobial [EPC],Quinolones [Chemical/Ingredient] |
