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ofloxacin
ofloxacin - 67877-227-55 - (ofloxacin)
Drug Information of ofloxacin
| Product NDC: | 67877-227 |
| Proprietary Name: | ofloxacin |
| Non Proprietary Name: | ofloxacin |
| Active Ingredient(s): | 3 mg/mL & nbsp; ofloxacin |
| Administration Route(s): | OPHTHALMIC |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of ofloxacin
| Product NDC: | 67877-227 |
| Labeler Name: | Ascend Laboratories, LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA078559 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20110415 |
Package Information of ofloxacin
| Package NDC: | 67877-227-55 |
| Package Description: | 1 BOTTLE, PLASTIC in 1 CARTON (67877-227-55) > 5 mL in 1 BOTTLE, PLASTIC |
NDC Information of ofloxacin
| NDC Code | 67877-227-55 |
| Proprietary Name | ofloxacin |
| Package Description | 1 BOTTLE, PLASTIC in 1 CARTON (67877-227-55) > 5 mL in 1 BOTTLE, PLASTIC |
| Product NDC | 67877-227 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | ofloxacin |
| Dosage Form Name | SOLUTION |
| Route Name | OPHTHALMIC |
| Start Marketing Date | 20110415 |
| Marketing Category Name | ANDA |
| Labeler Name | Ascend Laboratories, LLC |
| Substance Name | OFLOXACIN |
| Strength Number | 3 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Quinolone Antimicrobial [EPC],Quinolones [Chemical/Ingredient] |
