VIGAMOX
- Product NDC
- 50090-0859
- 11-digit product format
- 500900859
- Labeler code
- 50090
- Product ID
- 50090-0859_e5464878-ac2b-4c5f-9f54-279979ebe213
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- moxifloxacin hydrochloride
- Dosage form
- SOLUTION/ DROPS
- Route
- OPHTHALMIC
- Labeler
- A-S Medication Solutions
- Application
- NDA021598
- Marketing category
- NDA
- Marketing start
- 2003-05-07
- 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
- 2020-12-31
- 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 |
|---|
| 50090-0859-0 | 50090085900 | 1 BOTTLE, PLASTIC in 1 CARTON (50090-0859-0) > 3 mL in 1 BOTTLE, PLASTIC | 2014-11-28 | 0000-00-00 | No | No | Current |