Product NDC: | 54868-3923 |
Proprietary Name: | LEVAQUIN |
Non Proprietary Name: | levofloxacin |
Active Ingredient(s): | 500 mg/1 & nbsp; levofloxacin |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, FILM COATED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 54868-3923 |
Labeler Name: | Physicians Total Care, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA020634 |
Marketing Category: | NDA |
Start Marketing Date: | 20000511 |
Package NDC: | 54868-3923-7 |
Package Description: | 14 TABLET, FILM COATED in 1 BOTTLE (54868-3923-7) |
NDC Code | 54868-3923-7 |
Proprietary Name | LEVAQUIN |
Package Description | 14 TABLET, FILM COATED in 1 BOTTLE (54868-3923-7) |
Product NDC | 54868-3923 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | levofloxacin |
Dosage Form Name | TABLET, FILM COATED |
Route Name | ORAL |
Start Marketing Date | 20000511 |
Marketing Category Name | NDA |
Labeler Name | Physicians Total Care, Inc. |
Substance Name | LEVOFLOXACIN |
Strength Number | 500 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Quinolone Antimicrobial [EPC],Quinolones [Chemical/Ingredient] |