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LEVAQUIN
LEVAQUIN - 50458-930-06 - (levofloxacin)
Drug Information of LEVAQUIN
| Product NDC: | 50458-930 |
| Proprietary Name: | LEVAQUIN |
| Non Proprietary Name: | levofloxacin |
| Active Ingredient(s): | 750 mg/1 & nbsp; levofloxacin |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of LEVAQUIN
| Product NDC: | 50458-930 |
| Labeler Name: | Janssen Pharmaceuticals, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020634 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19961220 |
Package Information of LEVAQUIN
| Package NDC: | 50458-930-06 |
| Package Description: | 1 TABLET, FILM COATED in 1 BLISTER PACK (50458-930-06) |
NDC Information of LEVAQUIN
| NDC Code | 50458-930-06 |
| Proprietary Name | LEVAQUIN |
| Package Description | 1 TABLET, FILM COATED in 1 BLISTER PACK (50458-930-06) |
| Product NDC | 50458-930 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | levofloxacin |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 19961220 |
| Marketing Category Name | NDA |
| Labeler Name | Janssen Pharmaceuticals, Inc. |
| Substance Name | LEVOFLOXACIN |
| Strength Number | 750 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Quinolone Antimicrobial [EPC],Quinolones [Chemical/Ingredient] |
