Levofloxacin
- Product NDC
- 68071-4900
- 11-digit product format
- 680714900
- Labeler code
- 68071
- Product ID
- 68071-4900_bb919705-f8ff-4570-e053-2a95a90a18e1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Levofloxacin
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA201043
- Marketing category
- ANDA
- Marketing start
- 2011-06-20
- 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
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68071-4900-1 | 68071490001 | 10 TABLET, FILM COATED in 1 BOTTLE (68071-4900-1) | 2019-05-21 | 0000-00-00 | No | No | Current |