Moxifloxacin Hydrochloride
- Product NDC
- 60429-893
- 11-digit product format
- 604290893
- Labeler code
- 60429
- Product ID
- 60429-893_bbf31bd8-3c7e-574b-e053-2995a90a5ef7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Moxifloxacin Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Golden State Medical Supply, Inc.
- Application
- ANDA205348
- Marketing category
- ANDA
- Marketing start
- 2016-01-14
- 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
- 2022-12-31
- 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 |
|---|
| 60429-893-30 | 60429089330 | 30 TABLET in 1 BOTTLE (60429-893-30) | 30 tablet | 2017-10-09 | 0000-00-00 | No | No | Current |