Moxifloxacin
- Product NDC
- 55700-657
- 11-digit product format
- 557000657
- Labeler code
- 55700
- Product ID
- 55700-657_2468dc10-eb71-49b4-a857-31448c6c4bb8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Moxifloxacin
- Dosage form
- SOLUTION/ DROPS
- Route
- OPHTHALMIC
- Labeler
- Lake Erie Medical DBA Quality Care Products LLC
- Application
- ANDA202916
- Marketing category
- ANDA
- Marketing start
- 2018-07-20
- Marketing end
- 0000-00-00
- Substance
- MOXIFLOXACIN HYDROCHLORIDE
- Active strength
- 5 mg/mL
- Pharmacologic classes
- Quinolone Antimicrobial [EPC],Quinolones [CS]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record