moxifloxacin hydrochloride
- Product NDC
- 13668-201
- 11-digit product format
- 136680201
- Labeler code
- 13668
- Product ID
- 13668-201_c75617c7-dd3d-4819-98ec-3637b32a616c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- moxifloxacin hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Torrent Pharmaceuticals Limited
- Application
- ANDA200160
- Marketing category
- ANDA
- Marketing start
- 2014-04-03
- Marketing end
- 0000-00-00
- Substance
- MOXIFLOXACIN HYDROCHLORIDE
- Active strength
- 400 mg/1
- Pharmacologic classes
- Quinolone Antimicrobial [EPC], Quinolones [CS]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 13668-201-01 | 13668020101 | 100 TABLET in 1 BOTTLE (13668-201-01) | 100 tablet | 2014-04-03 | 0000-00-00 | No | No | Current |
| 13668-201-05 | 13668020105 | 500 TABLET in 1 BOTTLE (13668-201-05) | 500 tablet | 2014-04-03 | 0000-00-00 | No | No | Current |
| 13668-201-30 | 13668020130 | 30 TABLET in 1 BOTTLE (13668-201-30) | 30 tablet | 2014-04-03 | 0000-00-00 | No | No | Current |
| 13668-201-74 | 13668020174 | 100 TABLET in 1 CARTON (13668-201-74) | 100 tablet | 2014-04-03 | 0000-00-00 | No | No | Current |