Levofloxacin
- Product NDC
- 68071-3511
- 11-digit product format
- 680713511
- Labeler code
- 68071
- Product ID
- 68071-3511_2f8911a1-ac9b-6c6c-e063-6394a90a7ac5
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Levofloxacin
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA202801
- Marketing category
- ANDA
- Marketing start
- 2015-01-09
- Substance
- LEVOFLOXACIN
- Active strength
- 500 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 6GNT3Y5LMF | LEVOFLOXACIN | 138199-71-0 | LEVOFLOXACIN |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 68071-3511-5 | 68071351105 | 50 TABLET, FILM COATED in 1 BOTTLE (68071-3511-5) | 2023-09-20 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Levofloxacin | NuCare Pharmaceuticals,Inc. | 2025-03-04 | HUMAN PRESCRIPTION DRUG LABEL | 2 |