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Cipro
Cipro - 50419-773-01 - (ciprofloxacin)
Drug Information of Cipro
| Product NDC: | 50419-773 |
| Proprietary Name: | Cipro |
| Non Proprietary Name: | ciprofloxacin |
| Active Ingredient(s): | & nbsp; ciprofloxacin |
| Administration Route(s): | |
| Dosage Form(s): | KIT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Cipro
| Product NDC: | 50419-773 |
| Labeler Name: | Bayer HealthCare Pharmaceuticals Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020780 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19970926 |
Package Information of Cipro
| Package NDC: | 50419-773-01 |
| Package Description: | 1 KIT in 1 KIT (50419-773-01) * 100 mL in 1 BOTTLE, GLASS * 100 mL in 1 BOTTLE, GLASS |
NDC Information of Cipro
| NDC Code | 50419-773-01 |
| Proprietary Name | Cipro |
| Package Description | 1 KIT in 1 KIT (50419-773-01) * 100 mL in 1 BOTTLE, GLASS * 100 mL in 1 BOTTLE, GLASS |
| Product NDC | 50419-773 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | ciprofloxacin |
| Dosage Form Name | KIT |
| Route Name | |
| Start Marketing Date | 19970926 |
| Marketing Category Name | NDA |
| Labeler Name | Bayer HealthCare Pharmaceuticals Inc. |
| Substance Name | |
| Strength Number | |
| Strength Unit | |
| Pharmaceutical Classes |
