Avelox
- Product NDC
- 0085-1737
- 11-digit product format
- 000851737
- Labeler code
- 0085
- Product ID
- 0085-1737_9ae0561c-5e62-425f-a7f3-5cdbb842de80
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- moxifloxacin hydrochloride
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Schering Plough Corporation
- Application
- NDA021277
- Marketing category
- NDA
- Marketing start
- 2001-11-30
- Marketing end
- 0000-00-00
- Substance
- MOXIFLOXACIN HYDROCHLORIDE
- Active strength
- 400 mg/250mL
- Pharmacologic classes
- Quinolone Antimicrobial [EPC],Quinolones [CS]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record