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LEVAQUIN
LEVAQUIN - 10147-0941-6 - (levofloxacin)
Drug Information of LEVAQUIN
| Product NDC: | 10147-0941 |
| Proprietary Name: | LEVAQUIN |
| Non Proprietary Name: | levofloxacin |
| Active Ingredient(s): | 25 mg/mL & nbsp; levofloxacin |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of LEVAQUIN
| Product NDC: | 10147-0941 |
| Labeler Name: | Patriot Pharmaceuticals, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021721 |
| Marketing Category: | NDA AUTHORIZED GENERIC |
| Start Marketing Date: | 20130701 |
Package Information of LEVAQUIN
| Package NDC: | 10147-0941-6 |
| Package Description: | 1 BOTTLE in 1 CARTON (10147-0941-6) > 480 mL in 1 BOTTLE |
NDC Information of LEVAQUIN
| NDC Code | 10147-0941-6 |
| Proprietary Name | LEVAQUIN |
| Package Description | 1 BOTTLE in 1 CARTON (10147-0941-6) > 480 mL in 1 BOTTLE |
| Product NDC | 10147-0941 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | levofloxacin |
| Dosage Form Name | SOLUTION |
| Route Name | ORAL |
| Start Marketing Date | 20130701 |
| Marketing Category Name | NDA AUTHORIZED GENERIC |
| Labeler Name | Patriot Pharmaceuticals, Inc. |
| Substance Name | LEVOFLOXACIN |
| Strength Number | 25 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |
