Moxifloxacin Hydrochloride
- Product NDC
- 0093-7387
- 11-digit product format
- 000937387
- Labeler code
- 0093
- Product ID
- 0093-7387_4629423b-1b57-457c-8ae8-a8818389170b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Moxifloxacin Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Teva Pharmaceuticals USA, Inc.
- Application
- ANDA077437
- Marketing category
- ANDA
- Marketing start
- 2014-02-19
- 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0093-7387-56 | 00093738756 | 30 TABLET, FILM COATED in 1 BOTTLE (0093-7387-56) | 2014-02-19 | 0000-00-00 | No | No | Current |