Levofloxacin
- Product NDC
- 0121-0872
- 11-digit product format
- 001210872
- Labeler code
- 0121
- Product ID
- 0121-0872_a250dba6-497c-266e-e053-2995a90adcbf
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Levofloxacin
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- Pharmaceutical Associates, Inc.
- Application
- ANDA205222
- Marketing category
- ANDA
- Marketing start
- 2018-05-25
- Marketing end
- 0000-00-00
- Substance
- LEVOFLOXACIN
- Active strength
- 25 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0121-0872-20 | 00121087220 | 2 CASE in 1 CASE (0121-0872-20) > 4 TRAY in 1 CASE (0121-0872-40) > 10 CUP in 1 TRAY (0121-0872-10) > 10 mL in 1 CUP | 2 case | 2020-03-26 | 0000-00-00 | No | No | Current |