Levofloxacin
- Product NDC
- 0781-5792
- 11-digit product format
- 007815792
- Labeler code
- 0781
- Product ID
- 0781-5792_f03e9691-8fbe-4175-bc2e-5c627895bb71
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Levofloxacin
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Sandoz Inc
- Application
- ANDA077438
- Marketing category
- ANDA
- Marketing start
- 2011-06-20
- Marketing end
- 0000-00-00
- Substance
- LEVOFLOXACIN
- Active strength
- 750 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0781-5792-01 | 00781579201 | 100 TABLET, FILM COATED in 1 BOTTLE (0781-5792-01) | 2011-06-20 | 0000-00-00 | No | No | Current |
| 0781-5792-10 | 00781579210 | 1000 TABLET, FILM COATED in 1 BOTTLE (0781-5792-10) | 2011-06-20 | 0000-00-00 | No | No | Current |
| 0781-5792-20 | 00781579220 | 20 TABLET, FILM COATED in 1 BOTTLE (0781-5792-20) | 2011-06-20 | 0000-00-00 | No | No | Current |
| 0781-5792-50 | 00781579250 | 50 TABLET, FILM COATED in 1 BOTTLE (0781-5792-50) | 2011-06-20 | 0000-00-00 | No | No | Current |