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Cipro
Cipro - 50419-754-01 - (ciprofloxacin hydrochloride)
Drug Information of Cipro
| Product NDC: | 50419-754 |
| Proprietary Name: | Cipro |
| 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 Cipro
| Product NDC: | 50419-754 |
| Labeler Name: | Bayer HealthCare Pharmaceuticals Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA019537 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19871022 |
Package Information of Cipro
| Package NDC: | 50419-754-01 |
| Package Description: | 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50419-754-01) |
NDC Information of Cipro
| NDC Code | 50419-754-01 |
| Proprietary Name | Cipro |
| Package Description | 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50419-754-01) |
| Product NDC | 50419-754 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | ciprofloxacin hydrochloride |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 19871022 |
| Marketing Category Name | NDA |
| Labeler Name | Bayer HealthCare Pharmaceuticals Inc. |
| Substance Name | CIPROFLOXACIN HYDROCHLORIDE |
| Strength Number | 500 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Quinolone Antimicrobial [EPC],Quinolones [Chemical/Ingredient] |
