Levofloxacin
- Product NDC
- 42708-122
- 11-digit product format
- 427080122
- Labeler code
- 42708
- Product ID
- 42708-122_bc7bd03f-d67c-cb95-e053-2995a90abb21
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Levofloxacin
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- QPharma Inc
- Application
- ANDA201043
- 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
- 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 |
|---|
| 42708-122-07 | 42708012207 | 7 TABLET, FILM COATED in 1 BOTTLE (42708-122-07) | 2018-04-20 | 0000-00-00 | Yes | No | Current |