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Ciprofloxacin
Ciprofloxacin - 16571-135-10 - (Ciprofloxacin)
Drug Information of Ciprofloxacin
| Product NDC: | 16571-135 |
| Proprietary Name: | Ciprofloxacin |
| Non Proprietary Name: | Ciprofloxacin |
| Active Ingredient(s): | 3 mg/mL & nbsp; Ciprofloxacin |
| Administration Route(s): | OPHTHALMIC; TOPICAL |
| Dosage Form(s): | SOLUTION/ DROPS |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Ciprofloxacin
| Product NDC: | 16571-135 |
| Labeler Name: | Pack Pharmaceuticals, LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA077568 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20100915 |
Package Information of Ciprofloxacin
| Package NDC: | 16571-135-10 |
| Package Description: | 1 BOTTLE, PLASTIC in 1 CARTON (16571-135-10) > 10 mL in 1 BOTTLE, PLASTIC |
NDC Information of Ciprofloxacin
| NDC Code | 16571-135-10 |
| Proprietary Name | Ciprofloxacin |
| Package Description | 1 BOTTLE, PLASTIC in 1 CARTON (16571-135-10) > 10 mL in 1 BOTTLE, PLASTIC |
| Product NDC | 16571-135 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Ciprofloxacin |
| Dosage Form Name | SOLUTION/ DROPS |
| Route Name | OPHTHALMIC; TOPICAL |
| Start Marketing Date | 20100915 |
| Marketing Category Name | ANDA |
| Labeler Name | Pack Pharmaceuticals, LLC |
| Substance Name | CIPROFLOXACIN HYDROCHLORIDE |
| Strength Number | 3 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Quinolone Antimicrobial [EPC],Quinolones [Chemical/Ingredient] |
