levofloxacin
- Product NDC
- 48792-7816
- 11-digit product format
- 487927816
- Labeler code
- 48792
- Product ID
- 48792-7816_823c1490-c91a-c1d4-e053-2a91aa0ab872
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- levofloxacin
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Sunshine Lake Pharma CO., LTD.
- Application
- ANDA204968
- Marketing category
- ANDA
- Marketing start
- 2019-02-19
- Marketing end
- 0000-00-00
- Substance
- LEVOFLOXACIN
- Active strength
- 750 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 48792-7816-1 | 48792781601 | 20 TABLET, FILM COATED in 1 BOTTLE (48792-7816-1) | 2019-02-19 | 0000-00-00 | No | No | Current |