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Ofloxacin
Ofloxacin - 0093-7182-01 - (Ofloxacin)
Drug Information of Ofloxacin
| Product NDC: | 0093-7182 |
| Proprietary Name: | Ofloxacin |
| Non Proprietary Name: | Ofloxacin |
| Active Ingredient(s): | 400 mg/1 & nbsp; Ofloxacin |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Ofloxacin
| Product NDC: | 0093-7182 |
| Labeler Name: | Teva Pharmaceuticals USA Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA076182 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20040128 |
Package Information of Ofloxacin
| Package NDC: | 0093-7182-01 |
| Package Description: | 100 TABLET, FILM COATED in 1 BOTTLE (0093-7182-01) |
NDC Information of Ofloxacin
| NDC Code | 0093-7182-01 |
| Proprietary Name | Ofloxacin |
| Package Description | 100 TABLET, FILM COATED in 1 BOTTLE (0093-7182-01) |
| Product NDC | 0093-7182 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Ofloxacin |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20040128 |
| Marketing Category Name | ANDA |
| Labeler Name | Teva Pharmaceuticals USA Inc |
| Substance Name | OFLOXACIN |
| Strength Number | 400 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Quinolone Antimicrobial [EPC],Quinolones [Chemical/Ingredient] |
