Levofloxacin
- Product NDC
- 70934-050
- 11-digit product format
- 709340050
- Labeler code
- 70934
- Product ID
- 70934-050_b8a24f8e-fcac-5961-e053-2995a90a5e3f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Levofloxacin
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Denton Pharma, Inc. DBA Northwind Pharmaceuticals
- Application
- ANDA202801
- Marketing category
- ANDA
- Marketing start
- 2017-12-05
- Marketing end
- 0000-00-00
- Substance
- LEVOFLOXACIN
- Active strength
- 500 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70934-050-07 | 70934005007 | 7 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-050-07) | 2017-12-20 | 0000-00-00 | No | No | Current |
| 70934-050-10 | 70934005010 | 10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-050-10) | 2017-12-05 | 0000-00-00 | No | No | Current |
| 70934-050-14 | 70934005014 | 14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-050-14) | 2018-06-14 | 0000-00-00 | No | No | Current |